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YOSHINO Ken-ichiBiosignal Research CenterAssistant Professor
Researcher basic information
■ Research Keyword- mass spectrometry
- Protein Mass Spectrometry
- マススペクトロメトリー関係用語
- 翻訳後修飾
- mammallian Target of Rapamycin
- 細菌毒素
- 精子活性化ペプチド
■ Committee History
- May 2023 - Present, 一般社団法人日本質量分析学会, 理事
- Apr. 2012 - Present, 神戸大学, 六甲台地区事業場 衛生管理者
- Apr. 2005 - Present, 日本質量分析学会, 用語委員
- May 2017 - Jun. 2021, 一般社団法人日本質量分析学会, 理事
- Apr. 2011 - Mar. 2015, 日本質量分析学会, 委員(運営委員)
- Jun. 2013 - Mar. 2014, 高速液体クロマトグラフィー質量分析通則JIS改正原案作成委員会, 委員
- Apr. 2005 - Mar. 2009, 日本質量分析学会, 会誌編集委員長
- Apr. 2005 - Mar. 2009, 日本質量分析学会, 委員(運営委員)
- Apr. 2003 - Mar. 2007, 日本質量分析学会, 広報委員
Research activity information
■ Award- May 2006 The Mass Spectrometry Society of Japan, JMSSJ Award for Exellent Article, J. Mass Spectrom. Soc. Jpn. 52, 106-129 (2004)
- May 2003 社団法人日本肝臓学会, AJINOMOTO Award
- Oct. 1988 日本動物学会, Zoological Science Award
- Elsevier BV, Feb. 2024, Parasitology International, 100, 102864 - 102864, English, International magazine[Refereed]Scientific journal
- Protein homeostasis, including protein folding, refolding, and degradation, is thought to decline with aging. HSPB5 (also known as αB-crystallin) prevents target protein aggregation as a molecular chaperone and exhibits a cytoprotective function against various cell stresses. To elucidate the effect of HSPB5 on endoplasmic reticulum (ER) stress, we searched for novel binding proteins of HSPB5 using the proximity-dependent biotin labeling method. Proteins presumed to interact with HSPB5 in cells treated with the proteasome inhibitor MG132 were identified by a reversible biotin-binding capacity method combining tamavidin2-REV magnetic beads and mass spectrometry. We discovered a new binding protein for HSPB5, polo-like kinase 2 (PLK2), which is an apoptosis-related enzyme. The expression of PLK2 was upregulated by MG132 treatment, and it was co-localized with HSPB5 near the ER in L6 muscle cells. Inhibition of PLK2 decreased ER stress-induced phosphorylation of serine 19 in HSPB5 and increased apoptosis by activation of caspase 3 under ER stress. Overexpression of HSPB5 (WT) suppressed the ER stress-induced caspase 3 activity, but this was not observed with phospho-deficient HSPB5 (3A) mutants. These results clarify the role of HSPB5 phosphorylation during ER stress and suggest that the PLK2/HSPB5 pathway plays an essential role in cytoprotection against proteasome inhibition-induced ER stress.Sep. 2022, Int. J. Mol. Sci., 23(19) (19), 11257, English, International magazine, Co-authored internationally[Refereed]Scientific journal
- Japanese Black cattle (Japanese Wagyu) have a unique phenotype in which ectopic intramuscular fat accumulates in skeletal muscle, producing finely marbled beef. However, the mechanism of intramuscular fat formation in Japanese Black cattle remains unclear. To investigate the key genes involved in intramuscular fat accumulation, we comprehensively analyzed mRNA levels in subcutaneous and intramuscular fat tissues using RNA sequence (RNA-seq) analysis, which detected 27,606 genes. We identified eight key genes, namely carboxypeptidase E, tenascin C, transgelin, collagen type IV alpha 5 (COL4A5), cysteine and glycine-rich protein 2, PDZ, and LIM domain 3, phosphatase 1 regulatory inhibitor subunit 14A, and regulator of calcineurin 2. These genes were highly and specifically expressed in intramuscular fat tissue. Immunohistochemical analysis revealed a collagen network, including COL4A5, in the basement membrane around the intramuscular fat tissue. Moreover, pathway analysis revealed that, in intramuscular fat tissue, differentially expressed genes are related to cell adhesion, proliferation, and cancer pathways. Furthermore, pathway analysis showed that the transforming growth factor-β (TGF-β) and small GTPases regulators RASGRP3, ARHGEF26, ARHGAP10, ARHGAP24, and DLC were upregulated in intramuscular fat. Our study suggests that these genes are involved in intramuscular fat formation in Japanese Black cattle.MDPI AG, Jul. 2021, Genes, 12(8) (8), 1107, English, International magazine[Refereed]Scientific journal
- The Mass Spectrometry Society of Japan, Feb. 2021, Journal of the Mass Spectrometry Society of Japan, 69(1) (1), 8 - 19, Japanese[Refereed]Scientific journal
- Branched-chain polyamine synthase (BpsA) catalyzes sequential aminopropyl transfer from the donor, decarboxylated S-adenosylmethionine (dcSAM), to the acceptor, linear-chain polyamine, resulting in the production of a quaternary-branched polyamine via tertiary branched polyamine intermediates. Here, we analyzed the catalytic properties and X-ray crystal structure of Tth-BpsA from Thermus thermophilus and compared them with those of Tk-BpsA from Thermococcus kodakarensis, which revealed differences in acceptor substrate specificity and C-terminal structure between these two enzymes. To investigate the role of the C-terminal flexible region in acceptor recognition, a region (QDEEATTY) in Tth-BpsA was replaced with that in Tk-BpsA (YDDEESSTT) to create chimeric Tth-BpsA C9, which showed a severe reduction in catalytic efficiency toward N4 -aminopropylnorspermidine, but not toward N4 -aminopropylspermidine, mimicking Tk-BpsA substrate specificity. Tth-BpsA C9 Tyr346 and Thr354 contributed to discrimination between tertiary branched-chain polyamine substrates, suggesting that the C-terminal region of BpsA recognizes acceptor substrates. Liquid chromatography-tandem mass spectrometry analysis on a Tk-BpsA reaction mixture with dcSAM revealed two aminopropyl groups bound to two of five aspartate/glutamate residues (Glu339 , Asp342 , Asp343 , Glu344 , and Glu345 ) in the C-terminal flexible region. Mutating each of these five amino acid residues to asparagine/glutamine resulted in a slight decrease in activity. The quadruple mutant D342N/D343N/E344Q/E345Q exhibited a severe reduction in catalytic efficiency, suggesting that these aspartate/glutamate residues function to receive aminopropyl chains. In addition, the X-ray crystal structure of the Tk-BpsA ternary complex bound to N4 -bis(aminopropyl)spermidine revealed that Asp126 and Glu259 interacted with the aminopropyl moiety in N4 -aminopropylspermidine.Oct. 2019, The FEBS Journal, 286(19) (19), 3926 - 3940, English, International magazine[Refereed]Scientific journal
- Society for Neuroscience, Jan. 2018, The Journal of Neuroscience, 38(2) (2), 278 - 290, English, International magazine[Refereed]Scientific journal
- Oct. 2016, Nucleic acids research, 44(18) (18), 8704 - 8713, English, International magazine[Refereed]Scientific journal
- Jun. 2016, Microbiology and immunology, 60(6) (6), 407 - 417, English, International magazine[Refereed]Scientific journal
- In mammalian nucleotide excision repair, the DDB1-DDB2 complex recognizes UV-induced DNA photolesions and facilitates recruitment of the XPC complex. Upon binding to damaged DNA, the Cullin 4 ubiquitin ligase associated with DDB1-DDB2 is activated and ubiquitinates DDB2 and XPC. The structurally disordered N-terminal tail of DDB2 contains seven lysines identified as major sites for ubiquitination that target the protein for proteasomal degradation; however, the precise biological functions of these modifications remained unknown. By exogenous expression of mutant DDB2 proteins in normal human fibroblasts, here we show that the N-terminal tail of DDB2 is involved in regulation of cellular responses to UV. By striking contrast with behaviors of exogenous DDB2, the endogenous DDB2 protein was stabilized even after UV irradiation as a function of the XPC expression level. Furthermore, XPC competitively suppressed ubiquitination of DDB2 in vitro, and this effect was significantly promoted by centrin-2, which augments the DNA damage-recognition activity of XPC. Based on these findings, we propose that in cells exposed to UV, DDB2 is protected by XPC from ubiquitination and degradation in a stochastic manner; thus XPC allows DDB2 to initiate multiple rounds of repair events, thereby contributing to the persistence of cellular DNA repair capacity.Feb. 2015, Nucleic acids research, 43(3) (3), 1700 - 1713, English, International magazine[Refereed]Scientific journal
- 2015, Bioscience, biotechnology, and biochemistry, 79(11) (11), 1867 - 1875, English, International magazine[Refereed]Scientific journal
- Jul. 2014, The Journal of neuroscience : the official journal of the Society for Neuroscience, 34(28) (28), 9268 - 9280, English, International magazine[Refereed]Scientific journal
- Apr. 2013, Journal of biomedical science, 20, 24 - 24, English, International magazine[Refereed]Scientific journal
- Sep. 2012, Molecular biology of the cell, 23(18) (18), 3707 - 3721, English, International magazine[Refereed]Scientific journal
- Feb. 2012, The Journal of biological chemistry, 287(8) (8), 5507 - 5517, English, International magazine[Refereed]Scientific journal
- BACKGROUND: Chaperone-mediated autophagy (CMA) is a selective autophagy-lysosome protein degradation pathway. The role of CMA in normal neuronal functions and in neural disease pathogenesis remains unclear, in part because there is no available method to monitor CMA activity at the single-cell level. METHODOLOGY/PRINCIPAL FINDINGS: We sought to establish a single-cell monitoring method by visualizing translocation of CMA substrates from the cytosol to lysosomes using the HaloTag (HT) system. GAPDH, a CMA substrate, was fused to HT (GAPDH-HT); this protein accumulated in the lysosomes of HeLa cells and cultured cerebellar Purkinje cells (PCs) after labeling with fluorescent dye-conjugated HT ligand. Lysosomal accumulation was enhanced by treatments that activate CMA and prevented by siRNA-mediated knockdown of LAMP2A, a lysosomal receptor for CMA, and by treatments that inactivate CMA. These results suggest that lysosomal accumulation of GAPDH-HT reflects CMA activity. Using this method, we revealed that mutant γPKC, which causes spinocerebellar ataxia type 14, decreased CMA activity in cultured PCs. CONCLUSION/SIGNIFICANCE: In the present study, we established a novel fluorescent-based method to evaluate CMA activity in a single neuron. This novel method should be useful and valuable for evaluating the role of CMA in various neuronal functions and neural disease pathogenesis.2012, PloS one, 7(2) (2), e31232, English, International magazine[Refereed]Scientific journal
- Apr. 2011, Molecular biology of the cell, 22(8) (8), 1340 - 52, English, International magazine[Refereed]Scientific journal
- Feb. 2010, Molecular and cellular biology, 30(4) (4), 1049 - 58, English, International magazine[Refereed]Scientific journal
- Oct. 2009, Analytical biochemistry, 393(2) (2), 248 - 54, English, International magazine[Refereed]Scientific journal
- Feb. 2009, Genes to cells : devoted to molecular & cellular mechanisms, 14(2) (2), 179 - 89, English, International magazine[Refereed]Scientific journal
- Feb. 2008, The Journal of Biological Chemistry, 283(7) (7), 4430 - 4438, English, International magazine[Refereed]Scientific journal
- Sep. 2007, Biochemical and biophysical research communications, 361(1) (1), 218 - 23, English, International magazine[Refereed]Scientific journal
- Jul. 2007, The Journal of biological chemistry, 282(28) (28), 20329 - 39, English, International magazine[Refereed]Scientific journal
- Oct. 2006, The Journal of biological chemistry, 281(42) (42), 31627 - 37, English, International magazine[Refereed]Scientific journal
- Jul. 2006, Genes to cells : devoted to molecular & cellular mechanisms, 11(7) (7), 757 - 66, English, International magazine[Refereed]Scientific journal
- Mar. 2006, Journal of Biochemistry, 139(3) (3), 347 - 354, English, International magazine[Refereed]Scientific journal
- Jan. 2006, Journal of biochemistry, 139(1) (1), 129 - 135, English, International magazine[Refereed]Scientific journal
- Jan. 2006, FEMS microbiology letters, 254(1) (1), 157 - 64, English, International magazine[Refereed]Scientific journal
- Biochemical and morphologic evidence of the interaction of oligodendrocyte membrane rafts with actin filaments.Cytoskeletal structures under the cell membrane carry out pivotal roles in the maintenance and remodeling of the cell structures. Reforming of the cytoskeletal networks after partial extraction of membrane components could be a good clue to identify molecular components pertaining the interaction of cytoskeleton with membrane. A detergent extract from 3-week-old rat brain membrane fraction was found to make an actin-based gel upon incubation at 25 degrees C. Some protein components of the gelation products were recovered in a Triton-insoluble low-density microdomain fraction (raft) after depolymerization of actin filaments. Some of these proteins were identified as 2',3'-cyclic nucleotide-3'-phosphodiesterase (CNPase), proteolipid protein (PLP), and myelin oligodendrocyte glycoprotein (MOG) through electrospray time-of-flight (ESI-TOF) analysis and Western blotting. Because these proteins are well-known marker proteins of oligodendrocytes, localization of these proteins and cholesterol, a raft-localized lipid, with actin filaments was studied using cultured oligodendrocytes. Clear colocalization of these proteins and cholesterol with actin filaments was observed after Triton treatment at 4 degrees C before fixation. These results indicate that raft microdomains participate in the formation of cell shape through interaction with microfilaments in oligodendrocytes.Jul. 2005, Journal of neuroscience research, 81(2) (2), 218 - 225, English, International magazine[Refereed]Scientific journal
- Apr. 2005, The Journal of biological chemistry, 280(15) (15), 15029 - 37, English, International magazine[Refereed]Scientific journal
- Apr. 2005, Journal of Biochemistry, 137(4) (4), 509 - 515, English, International magazine[Refereed]
- Dissociation of raptor from mTOR is a mechanism of rapamycin-induced inhibition of mTOR function.The mammalian target of rapamycin (mTOR) is a Ser/Thr protein kinase that plays a crucial role in a nutrient-sensitive signalling pathway that regulates cell growth. TOR signalling is potently inhibited by rapamycin, through the direct binding of a FK506-binding protein 12 (FKBP12)/rapamycin complex to the TOR FRB domain, a segment amino terminal to the kinase catalytic domain. The molecular basis for the inhibitory action of FKBP12/rapamycin remains uncertain. Raptor (regulatory associated protein of mTOR) is a recently identified mTOR binding partner that is essential for mTOR signalling in vivo, and whose binding to mTOR is critical for mTOR-catalysed substrate phosphorylation in vitro. Here we investigated the stability of endogenous mTOR/raptor complex in response to rapamycin in vivo, and to the direct addition of a FKBP12/rapamycin complex in vitro. Rapamycin diminished the recovery of endogenous raptor with endogenous or recombinant mTOR in vivo; this inhibition required the ability of mTOR to bind the FKBP12/rapamycin complex, but was independent of mTOR kinase activity. Rapamycin, in the presence of FKBP12, inhibited the association of raptor with mTOR directly in vitro, and concomitantly reduced the mTOR-catalysed phosphorylation of raptor-dependent, but not raptor-independent substrates; mTOR autophosphorylation was unaltered. These observations indicate that rapamycin inhibits mTOR function, at least in part, by inhibiting the interaction of raptor with mTOR; this action uncouples mTOR from its substrates, and inhibits mTOR signalling without altering mTOR's intrinsic catalytic activity.Apr. 2004, Genes to cells : devoted to molecular & cellular mechanisms, 9(4) (4), 359 - 366, English, International magazine[Refereed]Scientific journal
- Protein-tyrosine phosphatase alpha, RPTP alpha, is a Helicobacter pylori VacA receptor.Helicobacter pylori vacuolating cytotoxin, VacA, induces vacuolation, mitochondrial damage, cytochrome c release, and apoptosis of gastric epithelial cells. To detect gastric proteins that serve as VacA receptors, we used VacA co-immunoprecipitation techniques following biotinylation of the cell surface and identified p250, a receptor-like protein-tyrosine phosphatase beta (RPTP beta) as a VacA-binding protein (Yahiro, K., Niidome, T., Kimura, M., Hatakeyama, T., Aoyagi, H., Kurazono, H., Imagawa, K., Wada, A., Moss, J., and Hirayama, T. (1999) J. Biol. Chem. 274, 36693-36699). VacA causes vacuolation of G401 cells, a human kidney tumor cell line, although they do not express RPTP beta. By co-immunoprecipitation with VacA, we identified p140 as a potential receptor in those cells. p140 purified by chromatography on a peanut agglutinin affinity matrix contained internal amino acid sequences of RGEENTDYVNASFIDGYRQK and AEGILDVFQTVK, which are identical to those in RPTP alpha. The peptide mass fingerprinting of p140 by time of flight-MS analysis also supported this identification. Treatment of G401 cells with RPTP alpha-morpholino antisense oligonucleotide before exposure to toxin inhibited vacuolation. These data suggest that RPTP alpha acts as a receptor for VacA in G401 cells. Thus, two receptor tyrosine phosphatases, RPTP alpha and RPTP beta, serve as VacA receptors.May 2003, The Journal of biological chemistry, 278(21) (21), 19183 - 19189, English, International magazine[Refereed]Scientific journal
- May 2003, The Journal of biological chemistry, 278(18) (18), 15461 - 4, English, International magazine[Refereed]Scientific journal
- Inhibition of amino acid-mTOR signaling by a leucine derivative induces G1 arrest in Jurkat cells.We have previously demonstrated that N-acetylleucine amide, a derivative of L-leucine, inhibits leucine-induced p70(S6k) activation in a rat hepatoma cell line. In the present study, we investigated whether N-acetylleucine amide is capable of inhibiting amino acid-mTOR signaling. N-Acetylleucine amide caused cell cycle arrest at G1 stage in Jurkat cells, a human leukemia T cell line, concomitant with the inhibition of serum-induced p70(S6k) activation and p27 degradation. Treatment of Jurkat cells with this compound also exhibited dephosphorylation of retinoblastoma protein. These effects are similar to the inhibitory effects of rapamycin on amino acid-mTOR signaling pathway and suggest that N-acetylleucine amide acts as a rapamycin-like reagent to inhibit cell cycle progression in Jurkat cells.Feb. 2003, Biochemical and biophysical research communications, 301(2) (2), 417 - 423, English, International magazine[Refereed]Scientific journal
- A possible linkage between AMP-activated protein kinase (AMPK) and mammalian target of rapamycin (mTOR) signalling pathway.BACKGROUND: The mammalian target of rapamycin (mTOR) regulates multiple cellular functions including translation in response to nutrients, especially amino acids. AMP-activated protein kinase (AMPK) modulates metabolism in response to energy demand by responding to changes in AMP. RESULTS: The treatment of SV40-immortalized human corneal epithelial cells (HCE-T cells) with 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), widely used as an AMPK activator, inhibits p70 S6k activities. Altered glucose availability, which regulates AMPK activity, also modulates the activity of p70 S6k. AICAR treatment also inhibits phosphorylation of Thr-412 in the p70 S6 kinase (p70 S6k), which is indispensable for the activity. Furthermore, over-expression of mutant AMPK subunits by stable expression in rabbit pulmonary fibroblast cell lines (PS120 cells) also modulates p70 S6k activity. The insensitivity of the rapamycin-resistant p70 S6k variant to AICAR treatment suggests that the inhibition of p70 S6k is mediated through a common effector, supporting a model whereby mTOR and its downstream effector are controlled by AMPK. CONCLUSION: These results indicate that the AMPK and mTOR signalling pathways are possibly linked. In addition to the mTOR signal acting as a priming switch that modulates p70 S6k activation, AMPK appears to provide an overriding switch linking p70 S6k regulation to cellular energy metabolism.Jan. 2003, Genes to Cells, 8(1) (1), 65 - 79, English, International magazine[Refereed]Scientific journal
- Tag-mediated isolation of yeast mitochondrial ribosome and mass spectrometric identification of its new components.Mitochondrial ribosomal proteins (mrps) of the budding yeast, Saccharomyces cerevisiae, have been extensively characterized genetically and biochemically. However, the list of the genes encoding individual mrps is still not complete and quite a few of the mrps are only predicted from their similarity to bacterial ribosomal proteins. We have constructed a yeast strain in which one of the small subunit proteins, termed Mrp4, was tagged with S-peptide and used for affinity purification of mitochondrial ribosome. Mass spectrometric analysis of the isolated proteins detected most of the small subunit mrps which were previously identified or predicted and about half of the large subunit mrps. In addition, several proteins of unknown function were identified. To confirm their identity further, we added tags to these proteins and analyzed their localization in subcellular fractions. Thus, we have newly established Ymr158w (MrpS8), Ypl013c (MrpS16), Ymr188c (MrpS17) and Ygr165w (MrpS35) as small subunit mrps and Img1, Img2, Ydr116c (MrpL1), Ynl177c (MrpL22), Ynr022c (MrpL50) and Ypr100w (MrpL51) as large subunit mrps.Nov. 2002, European Journal of Biochemistry, 269(21) (21), 5203 - 5214, English, International magazine[Refereed]Scientific journal
- Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action.mTOR controls cell growth, in part by regulating p70 S6 kinase alpha (p70alpha) and eukaryotic initiation factor 4E binding protein 1 (4EBP1). Raptor is a 150 kDa mTOR binding protein that also binds 4EBP1 and p70alpha. The binding of raptor to mTOR is necessary for the mTOR-catalyzed phosphorylation of 4EBP1 in vitro, and it strongly enhances the mTOR kinase activity toward p70alpha. Rapamycin or amino acid withdrawal increases, whereas insulin strongly inhibits, the recovery of 4EBP1 and raptor on 7-methyl-GTP Sepharose. Partial inhibition of raptor expression by RNA interference (RNAi) reduces mTOR-catalyzed 4EBP1 phosphorylation in vitro. RNAi of C. elegans raptor yields an array of phenotypes that closely resemble those produced by inactivation of Ce-TOR. Thus, raptor is an essential scaffold for the mTOR-catalyzed phosphorylation of 4EBP1 and mediates TOR action in vivo.Jul. 2002, Cell, 110(2) (2), 177 - 189, English, International magazine[Refereed]Scientific journal
- Proteome and transcriptome analysis of the virulence genes regulated by the VirR/VirS system in Clostridium perfringens.The proteins under the control of the two-component system VirR/VirS in Clostridium perfringens were analyzed by using two-dimensional gel electrophoresis of the culture supernatant from the wild type and the virR mutant. Based on matrix-assisted laser desorption ionization-time of flight/mass spectrometry, seven positively regulated proteins and eight negatively regulated proteins were identified. Transcriptome analysis confirmed that 7 of the 15 proteins were regulated by the VirR/VirS system at the transcriptional level, but the remaining proteins were modified with a VirR/VirS-directed protease at the posttranslation and secretion levels. We purified and characterized the VirR/VirS-directed protease from the culture supernatant and identified it as a kind of clostripain. Because this proteolytic activity was strongly inhibited by leupeptin and antipain, it was concluded that this protease was a member of the family of cysteine proteases of C. perfringens.May 2002, Journal of bacteriology, 184(10) (10), 2587 - 2594, English, International magazine[Refereed]Scientific journal
- 2002, Proceedings 50th ASMS Conference on Mass Spectrometry and Allied Topics, 751 - 752, EnglishThe complete amino acid sequence determination of a novel protein by mass spectrometry with the tentative human consensus sequence databaseInternational conference proceedings
- Distinct regulatory mechanism for p70 S6 kinase beta from that for p70 S6 kinase alpha.BACKGROUND: A novel ribosomal S6 kinase, termed p70 S6 kinase beta (p70beta), has a highly homologous amino acid sequence to that of p70/p85 S6 kinase (p70alpha). This includes the critical phosphorylation sites, Thr252, Ser394 and Thr412 in p70alpha1, which correspond to Thr241, Ser383 and Thr401 in p70beta1, respectively. However, the regulatory mechanism for p70beta remains to be elucidated. RESULTS: We report here the expression and the mechanism of in vivo regulation of p70beta. Two isoforms, p70beta1 and p70beta2, were expressed in a variety of tissues at a different level. p70beta1 was mainly targeted to the nucleus, whereas p70beta2 dispersed throughout the cytoplasm including nucleoplasm. The kinase activity of p70beta1 was less sensitive to the inhibition induced by rapamycin, wortmannin and amino acid withdrawal than that of p70alpha. The portion of p70beta activity inhibited by rapamycin was rescued by the rapamycin-resistant mutant of the mammalian target of rapamycin (mTOR). Mutational analysis revealed that the phosphorylation of Thr241 and Thr401 in p70beta1 was indispensable for the kinase activity. In contrast, a p70beta1 mutant in which Ser383 was substituted with Gly (S383G) still retained nearly the half maximal activity. Sequential phosphorylation of wild-type and S383G mutant of p70beta1 with mTOR and 3-phosphoinositide-dependent protein kinase 1 (PDK1) in vitro synergistically activated their kinase activities. CONCLUSION: These results indicate that p70beta is regulated by the mTOR- and PDK1-signalling pathways through a synergistic interaction between phosphorylated Thr241 and Thr401, while Ser383 plays minor role in their activation mechanism. Activated p70beta may be less sensitive to dephosphorylation mediated by putative phosphatases activated by rapamycin, amino acid withdrawal, and probably wortmannin.Nov. 2001, Genes to Cells, 6(11) (11), 1003 - 1015, English, International magazine, Co-authored internationally[Refereed]Scientific journal
- Wiley, Sep. 2000, Genes to Cells, 5(9) (9), 765 - 775, English[Refereed]Scientific journal
- Mar. 2000, 小児感染免疫, 12(1) (1), 19 - 22, JapaneseA case of Salmonellosis with severe neurological impairment caused by Salmonella urbana (O30), which antigen is identical to the Escherichia coli O157 antigen[Refereed]Scientific journal
- 1999, Microbiology and Immunology, 43(4) (4), 331 - 337, English[Refereed]Scientific journal
- 1999, Journal of Neurochemistry, 72(1) (1), 327 - 337, English[Refereed]Scientific journal
- The antibodies against LPS of enterohemorrhagic Escherichia coli (EHEC) O157 in sera from patients infected with this organism and sera from healthy control subjects were examined by ELISA to investigate their immune response. Analysing these data, we found some heterogeneity of antibody response between adults and infants.The Japanese Association for Infectious Diseases, 1999, Kansenshogaku Zasshi, 73(8) (8), 772 - 777, Japanese
In healthy adults and children, the cutoff values for IgM antibodies to O157 LPS were calculated as 0.85, 0.40 and for IgG were as 0.57, 0.39 respectively. In patients, the ELISA values of adult were lower and decreased earlier than those of children. Therefore sero diagnosis for EHEC O157 infection for adult patients the timing of blood collection is very important. On the other hand, in some patients the sera of children showed a high level of IgM only 3 days from the onset. This tendency seemed to be related to severity of the disease. This immunological test was proved to be useless for healthy carriers because the antibodies against O157 LPS were not observed in their sera.[Refereed]Scientific journal - 日本小児感染症学会, Oct. 1998, 小児感染免疫, 10(3) (3), 227 - 227, Japanese, Domestic magazine急激に重症脳症に進展したサルモネラ感染症の1例[Refereed]Scientific journal
- Aug. 1998, Zoological Science, 15(4) (4), 507 - 516, English[Refereed]Scientific journal
- The Japanese Association for Infectious Diseases, Aug. 1998, Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases, 72(8) (8), 808 - 812, Japanese[Refereed]Scientific journal
- “QuixTM” is an immunochromato graphy-based direct detection kit for the E. coli O157 LPS antigen in the patient's stool. The present study was conducted to evaluate the efficacy of the kit for rapid diagnosis of enterohemorrhagic Escherichia coli (EHEC) O157 infection.The Japanese Association for Infectious Diseases, 1998, Kansenshogaku Zasshi, 72(8) (8), 834 - 839, Japanese, Domestic magazine
Sensitivity of the kit was determined using a pure culture of a clinical isolate of E. coli O157. Analytical sensitivity was found to be 5×105 CFU/ml. When compared with the culture method using fecal samples of 64 patients and with bloody diarrhea, sensitivity and specificity were 95.0%(19/20) and 86.4%(38/44), respectively, and overall agreement to culture method was 89.1%(57/64). One patient was found positive by culture method while negative in the present method, where the sample contained a low number of the cells less than the detection limit. Four of the six patients with a negative result by culture method and positive in the present method, were confirmed E. coli O157 infection by positive IgM antibody response against the E. coli O157 LPS. The discrepancy between the two methods seemed to be attributable to antibiotic adminis adminis-tration. In one patient, Salmonella urbana (O301302) was detected. The O301 antigen of this bacterium is well known to be identical to the E. coli O157 antigen.
When the present method was compared with an ELISA-based E. coli O157 LPS antigen detection kit, sensitivity and specificity were 100%(11/11) and 82.1%(23/28), and overall agreement to ELISA method was 87.2%(34/39).
From these findings, QuixTM is useful as a rapid diagnostic kit in the primary clinics, outpatient or bedside use. E. coli O157 LPS antigen in patient's fecal samples can be detected in about five minutes with this simple procedure. Early diagnosis using such a simple kit will largely contribute for the early treatment and prevention of severe complications of the E. coli O157 infection.[Refereed]Scientific journal - TAK-751S is a synthetic trisaccharide coupled to Chromosorb P using a spacer sequence of 8-methoxycarboyloctyl (MCO). Its chemical structure is similar to a human receptor (Gb3) of Stx produced by enterohemorrhagic Escherichia coli (EHEC). In vitro efficacy of TAK-715S was studied by using ACHN cultured cell assay, which is sensitive and specific for measuring low level of Stx.The Japanese Association for Infectious Diseases, 1998, Kansenshogaku Zasshi, 72(9) (9), 924 - 934, Japanese
Under various conditions, TAK-751S was mixed with purified Stx1 and Stx2, and residual free toxins in the solution were measured by using ACHN cells. TAK-715S was demonstrated to bind specifically to Stx1 and Stx2 under the condition similar to a human intestine while Chromsorb P did not bind to any Stx. The binding activity was stable in the presence of various processed foods, fresh vegetables and fruits. Antibiotics such as fosfomycin, kanamycin and norfloxacin did not disturb its binding capability. Minimum inhibitory concentrations of these antibiotics against Staphylococcus aureus FDA209P or E. coli NIH J JC-2 neither changed after incubating with TAK-751S for 60 min at 37°C.
These results suggest that TAK-751S can be given orally with various foods and antibiotics for the elimination of Stx1 and Stx2 in the gut of patients with EHEC infections.[Refereed]Scientific journal - Oct. 1997, Microbial Pathogenesis, 23(4) (4), 189 - 200, English[Refereed]Scientific journal
- Sep. 1997, 日本小児科学会雑誌, 101(9) (9), 1403 - 1407, Japanese, Domestic magazineA First Case of Hemolytic Uremic Syndrome Associated with Verotoxin-producing Escherichia coli O121:H19 in Japan[Refereed]Scientific journal
- Aug. 1997, FEBS Letters, 413(1) (1), 174 - 176, English[Refereed]Scientific journal
- Feb. 1997, Microbial Pathogenesis, 22(2) (2), 89 - 97, English[Refereed]Scientific journal
- Lead, Jul. 1996, FEBS Letters, 390(2) (2), 196 - 198, English, International magazine[Refereed]Scientific journal
- 1996, Rapid Communications in Mass Spectrometry, 10(6) (6), 637 - 640Scientific journal
- Lead, Apr. 1995, FEBS Letters, 362(3) (3), 319 - 322, English[Refereed]Scientific journal
- Lead, 1995, Journal of Clinical Microbiology, 33(12) (12), 3356 - 3358, English, International magazine, Co-authored internationally[Refereed]Scientific journal
- 1995, Contributions to Microbiology and Immunology, 13, 331 - 333, EnglishPurification and gene cloning of a superantigen (YPM) produced by a patient strain of Yersinia pseudotuberculosis.[Refereed]International conference proceedings
- 1995, Journal of Immunology, 154(11) (11), 5896 - 5906, EnglishSequence analysis of the gene for a novel superantigen produced by Yersinia pseudotuberculosis and expression of the recombinant protein[Refereed]Scientific journal
- Lead, 1995, Analytical Chemistry, 67(21) (21), 4028 - 4031, English[Refereed]Scientific journal
- Lead, Dec. 1994, FEBS Letters, 356(1) (1), 141 - 144, English[Refereed]Scientific journal
- Lead, Oct. 1994, Letters in Peptide Science, 1(2) (2), 95 - 105, English[Refereed]Scientific journal
- Apr. 1994, Development Growth & Differentiation, 36(2) (2), 209 - 221, English[Refereed]Scientific journal
- Lead, Jul. 1993, FEBS Letters, 326(1-3) (1-3), 83 - 86, English[Refereed]Scientific journal
- Lead, Elsevier BV, Aug. 1992, Comparative Biochemistry and Physiology Part B, 102(4) (4), 691 - 700, English[Refereed]Scientific journal
- Lead, Jun. 1992, European Journal of Biochemistry, 206(3) (3), 887 - 893, English[Refereed]Scientific journal
- Lead, Dec. 1991, FEBS Letters, 294(3) (3), 179 - 182, English[Refereed]Scientific journal
- Lead, Jun. 1991, Biochemistry, 30(25) (25), 6203 - 6209, English[Refereed]Scientific journal
- Nov. 1990, Biological Mass Spectrometry, 19(11) (11), 705 - 712, English[Refereed]Scientific journal
- Lead, 1990, Comparative Biochemistry and Physiology, 95B(2) (2), 423 - 429, English[Refereed]Scientific journal
- Lead, 1990, Comparative Biochemistry and Physiology, 97B(4) (4), 679 - 685, English[Refereed]Scientific journal
- Lead, 1989, Comparative Biochemistry and Physiology, 94B(4) (4), 739 - 751, English[Refereed]Scientific journal
- 1988, Comparative Biochemistry and Physiology, 89B(4) (4), 687 - 693, English[Refereed]Scientific journal
- 1988, Comparative Biochemistry and Physiology, 90C(2) (2), 305 - 311, English[Refereed]Scientific journal
- Zoological Society of Japan, Aug. 1987, Zoological Science, 4(4) (4), 649 - 656, English, International magazinePurification and structure of mosact and its derivatives from the egg jelly of the sea urchin Clypeaster japonicus[Refereed]Scientific journal
- Zoological Society of Japan, Aug. 1987, Zoological Science, 4(4) (4), 641 - 648, English, International magazine, Co-authored internationallySperact binds exclusively to sperm tails and causes an electrophoretic mobility shift in a major sperm tail protein of sea urchins[Refereed]Scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Jun. 2025, Journal of the Mass Spectrometry Society of Japan, 73(2) (2), 102 - 105, Japanese, Domestic magazine試験に出た質量分析(12)[変動範囲による原子量と同位体存在度の表記について][Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Jun. 2025, Journal of the Mass Spectrometry Society of Japan, 73(2) (2), 98 - 101, Japanese, Domestic magazine試験に出た質量分析(11)[The 38th International Chemistry Olympiad, Korea, 2006][Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Mar. 2025, Journal of the Mass Spectrometry Society of Japan, 73(1) (1), 45 - 48, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Dec. 2024, Journal of the Mass Spectrometry Society of Japan, 72(4) (4), 81 - 84, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Sep. 2024, Journal of the Mass Spectrometry Society of Japan, 72(3) (3), 46 - 49, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Jun. 2024, Journal of the Mass Spectrometry Society of Japan, 72(2) (2), 35 - 38, Japanese, International magazine[Refereed]Meeting report
- Lead, 一般社団法人日本質量分析学会, 01 Jun. 2024, Journal of the Mass Spectrometry Society of Japan, 72(2) (2), 27 - 30, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Mar. 2024, Journal of the Mass Spectrometry Society of Japan, 72(1) (1), 7 - 10, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Last, 一般社団法人日本質量分析学会, 01 Mar. 2024, Journal of the Mass Spectrometry Socitey of Japan, 72(1) (1), 4 - 6, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Dec. 2023, Journal of the Mass Spectrometry Society of Japan, 71(4) (4), 172 - 174, Japanese, Domestic magazine[Refereed]Meeting report
- Lead, 一般社団法人日本質量分析学会, 01 Sep. 2023, Journal of the Mass Spectrometry Society of Japan, 71(3) (3), 103 - 106, Japanese[Refereed][Invited]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Sep. 2023, Journal of the Mass Spectrometry Society of Japan, 71(3) (3), 128 - 131, Japanese, Domestic magazine[Refereed][Invited]Introduction scientific journal
- Lead, 01 Mar. 2023, 質量分析, 71(1) (1), 11 - 14, Japanese[Refereed]Introduction scientific journal
- Last, The Mass Spectrometry Society of Japan, 01 Mar. 2023, Journal of the Mass Spectrometry Society of Japan, 71(1) (1), 15 - 18, Japanese[Refereed]Introduction scientific journal
- The Mass Spectrometry Society of Japan, 01 Mar. 2022, Journal of the Mass Spectrometry Society of Japan, 70(1) (1), 85 - 89, JapaneseMeeting report
- Last, The Mass Spectrometry Society of Japan, 01 Mar. 2022, Journal of the Mass Spectrometry Society of Japan, 70(1) (1), 62 - 69, Japanese[Refereed]Introduction scientific journal
- Lead, 一般社団法人日本質量分析学会, 01 Oct. 2021, 質量分析, 69(5) (5), 98 - 99, Japanese, Domestic magazine[Invited]
- Last, 一般社団法人日本質量分析学会, 01 Oct. 2021, 質量分析, 69(5) (5), 114 - 137, Japanese, Domestic magazine中田尚男先生講演資料集Others
- Lead, The Mass Spectrometry Society of Japan, 01 Apr. 2021, Journal of the Mass Spectrometry Society of Japan, 69(2) (2), 30 - 33, Japanese[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Jun. 2018, Journal of the Mass Spectrometry Society of Japan, 66(3) (3), 142 - 147, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, Apr. 2018, Journal of the Mass Spectrometry Society of Japan, 66(2) (2), 107 - 115, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, Feb. 2018, Journal of the Mass Spectrometry Society of Japan, 66(1) (1), 43 - 48, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Jan. 2018, 和光純薬時報, 86(1) (1), 6 - 7, JapaneseTamavidin-REVを用いたタンパク質間相互作用の網羅的解析[Invited]Introduction other
- Lead, The Japanese Society for Analytical Chemistry, Jun. 2017, Benseki, 2017(6) (6), 216 - 223, Japanese, Domestic magazineAppropriate Usage of Analytical Instruments : Mass Spectrometry[Refereed][Invited]Introduction scientific journal
- The Mass Spectrometry Society of Japan, 2017, Journal of the Mass Spectrometry Society of Japan, 65(2) (2), 76 - 90, Japanese[Refereed]Introduction scientific journal
- (一社)日本神経学会, Dec. 2014, 臨床神経学, 54(Suppl.) (Suppl.), S242 - S242, JapanesePKCγKOパーキンソン症候群モデル βPIXリン酸化のドパミン遊離での役割
- IUPAC (International Union of Pure and Applied Chemistry) recommends that a hyphen, or, alternatively, a slash, should be used to indicate a combination of two analytical techniques such as liquid chromatography separation combined with mass spectrometry detection, in the last definitions of terms relating to mass spectrometry. Thus, such combined methods can be written as liquid chromatography-mass spectrometry or alternatively liquid chromatography/mass spectrometry. The corresponding abbreviations are LC-MS or LC/MS.The Mass Spectrometry Society of Japan, 01 Oct. 2014, Journal of the Mass Spectrometry Society of Japan, 62(5) (5), 61 - 64, Japanese[Refereed]Introduction scientific journal
- 2014, JOURNAL OF PHARMACOLOGICAL SCIENCES, 124, 207P - 207P, EnglishA protein kinase C-gamma knockout Parkinsonian model: Involvement of Pak-Interacting Exchange Factor-betaSummary international conference
- The "Definitions of terms relating to mass spectrometry [IUPAC (International Union of Pure and Applied Chemistry) recommendations 2013]" define the term "MS/MS spectrum" as "a mass spectrum obtained using tandem mass spectrometry." The semantic content of the term "MS/MS spectrum" is not only a product ion mass spectrum but also a precursor ion spectrum and a neutral loss spectrum. However, the term "MS/MS spectrum" is frequently used as a synonym of a product ion spectrum. An "MS/MS spectrum of the peptide angiotensin I" does not convey the same meaning as the "product ion spectrum of the peptide angiotensin I."The Mass Spectrometry Society of Japan, 2014, Journal of the Mass Spectrometry Society of Japan, 62(6) (6), 115 - 118, Japanese[Refereed]Introduction scientific journal
- Last, The Mass Spectrometry Society of Japan, Oct. 2013, Journal of the Mass Spectrometry Society of Japan, 61(5) (5), 47 - 52, Japanese, Domestic magazine[Refereed]Meeting report
- 日本臨床精神神経薬理学会・日本神経精神薬理学会, Oct. 2013, 日本臨床精神神経薬理学会・日本神経精神薬理学会合同年会プログラム・抄録集, 23回・43回, 249 - 249, Japanese蛍光イメージングを用いた神経細胞でのシャペロン介在性オートファジー活性の解析
- Aug. 2013, 生物工学会誌, 91(8) (8), 464 - 468, Japanese意外に知らない分子量と質量の単位の違い[Refereed][Invited]Introduction scientific journal
- 2013, JOURNAL OF PHARMACOLOGICAL SCIENCES, 121, 122P - 122P, EnglishAnalysis of PKCY substrates in nigro-striatum system:The role of beta PIX phosphorylation in the dopamine releaseSummary international conference
- (公社)日本薬理学会, Oct. 2012, 日本薬理学雑誌, 140(4) (4), 1P - 1P, Japanese黒質線条体系におけるPKCγの基質の解析
- 2012, 日本分子生物学会年会プログラム・要旨集(Web), 35th無細胞再構成系によるヌクレオチド除去修復活性制御因子の探索
- 2011, JOURNAL OF PHARMACOLOGICAL SCIENCES, 115, 247P - 247P, EnglishDoes mutant gamma PKC causing spinocerebellar ataxia type 14 (SCA14) affect chaperone-mediated autophagy (CMA)? -Attempt to measure CMA activity using a novel indicator-Summary international conference
- 化学同人, Dec. 2010, 化学, 65(12), 62-65(12) (12), 62 - 65, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~最終回[Refereed]Introduction scientific journal
- 化学同人, Nov. 2010, 化学, 65(11), 28-30(11) (11), 28 - 30, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑩[Refereed]Introduction scientific journal
- 化学同人, Sep. 2010, 化学, 65(9), 41-44(1) (1), 59 - 61, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑨[Refereed]Introduction scientific journal
- 化学同人, Aug. 2010, 化学, 65(8) (8), 56 - 59, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑧[Refereed][Invited]Introduction scientific journal
- 化学同人, Jul. 2010, 化学, 65(7), 56-58(7) (7), 56 - 58, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑦[Refereed]Introduction scientific journal
- In general, microchannel plate (MCP) is used as the detector for time-of-flight mass spectrometer (TOF-MS). In addition to the MCP, TOF-MS equipped with modified secondary electron multiplier (SEM) is commercially available. A superconducting tunnel junction (STJ) detector, which enables measurement of kinetic energy in addition to time-of-flight, has been developed for TOF-MS. MCP and SEM detectors give only m/z values, which remains ambiguous over charge number (z). Since kinetic energy is proportional to z, TOF-MS equipped with STJ detector is possible to determine mass (m) unambiguously. In this commentary, the features of MCP and modified SEM will be described. Furthermore, we give an outline of the STJ detector.The Mass Spectrometry Society of Japan, 01 Jun. 2010, Journal of the Mass Spectrometry Society of Japan, 58(3) (3), 111 - 116, Japanese[Refereed]Introduction scientific journal
- 化学同人, Jun. 2010, 化学, 65(6), 44-47(6) (6), 44 - 47, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑥[Refereed]Introduction scientific journal
- 科学評論社, Apr. 2010, Endocrinology, diabetology & metabolism, 30(4) (4), 377 - 385, JapanesePhosphopeptide analysis by LC/MS[n] with a linear ion trap mass spectrometerIntroduction scientific journal
- 化学同人, Apr. 2010, 化学, 65(4), 54-57(4) (4), 54 - 57, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~⑤[Refereed]Introduction scientific journal
- 化学同人, Mar. 2010, 化学, 65(3), 45-47(3) (3), 45 - 47, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~④[Refereed]Introduction scientific journal
- “MS” is an abbreviation for “mass spectrometry.” “Bunseki” and “Kaiseki” in Japanese are equivalent for “analysis” in English. A Japanese word “Sokutei” is for the English word “measurement.” Thus, the Japanese words “MS-Bunseki,” “MS-Kaiseki” and “MS-Sokutei” are redundant expressions.Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2010, Journal of the Mass Spectrometry Society of Japan, 58(1) (1), 29 - 34, JapaneseIntroduction scientific journal
- 化学同人, Feb. 2010, 化学, 65(2), 46-48(2) (2), 46 - 48, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~③[Refereed]Introduction scientific journal
- 2010, JOURNAL OF PHARMACOLOGICAL SCIENCES, 112, 54P - 54P, EnglishNovel phosphorylation site(s) of cofilin by PKC alpha and its role in the degranulation from RBL-2H3 mast cellsSummary international conference
- 2010, NEUROSCIENCE RESEARCH, 68, E196 - E196, EnglishSummary international conference
- 化学同人, Jan. 2010, 化学, 65(1), 59-61(1) (1), 59 - 61, Japaneseクイズで学ぶ用語の誤用~化学者なら専門用語も正確に~②[Refereed]Introduction scientific journal
- This is a mass spectrometry glossary recording of daily used “unofficial terms” which are not recorded in the official glossary. In addition, the misuse examples which ignore the definition of scientific terminology and the terms which become the obsolete words officially are recorded.Lead, The Mass Spectrometry Society of Japan, 01 Dec. 2009, Journal of the Mass Spectrometry Society of Japan, 57(6) (6), 379 - 385, Japanese[Refereed]Introduction scientific journal
- 公益社団法人 日本農芸化学会, 01 Jun. 2009, 化学と生物, 47(6) (6), 436 - 440, JapaneseIntroduction scientific journal
- Apr. 2009, 化学, 64(4) 43, Japaneseマススペクトルの横軸ラベルは"m/z"に限ります ~御用だ誤用だ! 「用語」の誤用、第12回Introduction scientific journal
- Mar. 2009, 化学, 64(3), 43, Japanese“TIC”はtotal ion chromatogramの略語にあらず!~御用だ誤用だ! 「用語」の誤用、第11回Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2009, Journal of the Mass Spectrometry Society of Japan, 57(1) (1), 37 - 39, Japanese[Refereed][Invited]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2009, Journal of the Mass Spectrometry Society of Japan, 57(1) (1), 40 - 41, Japanese[Refereed]Introduction scientific journal
- The delayed extraction (also known as pulsed extraction) technique involves the application of a time delay between the ionization pulse and an accelerating voltage pulse for desorption/ionization from a surface. This technique can achieve energy focusing in a matrix-assisted laser desorption/ionization (MALDI) time-of-flight (TOF) mass spectrometer and is used to improve mass resolving power. We explain the principles of delayed extraction (pulsed extraction) used in a MALDI TOF mass spectrometer.The Mass Spectrometry Society of Japan, 01 Feb. 2009, Journal of the Mass Spectrometry Society of Japan, 57(1) (1), 31 - 36, Japanese[Refereed]Introduction scientific journal
- Feb. 2009, 化学, 64(2), 23, Japaneseトリプシンは制限酵素にあらず! ~御用だ誤用だ! 「用語」の誤用、第10回Introduction scientific journal
- 2009, JOURNAL OF PHARMACOLOGICAL SCIENCES, 109, 236P - 236P, EnglishCofilin is phosphorylated by cPKC in the degranulation from RBL-2H3 mast cellsSummary international conference
- Jan. 2009, 化学, 64(1), 61, Japanese“Mass Spectrometer”は質量分析器にあらず ~御用だ誤用だ! 「用語」の誤用、第9回Introduction scientific journal
- By measurement of post-source decay (PSD) product ion mass spectrum, matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry (TOFMS) enable mass spectrometry/mass spectrometry (MS/MS)-like analysis to obtain structural information. We will explain the basics of MS/MS-like analysis in reflectron mode of MALDI TOFMS by comparing post-source decay product ion mass spectrum acquired by the standard reflectron and the curved field reflectron.The Mass Spectrometry Society of Japan, 01 Dec. 2008, Journal of the Mass Spectrometry Society of Japan, 56(6) (6), 263 - 268, Japanese[Refereed]Introduction scientific journal
- The unified atomic mass unit (unit symbol: u) is a non-SI unit of mass, defined as one-twelfth the mass of a single 12C atom in its ground state. [SI: Le Système International d'Unités; The International System of Units] This definition was agreed upon by both the International Union of Pure and Applied Physics (IUPAP) and the International Union of Pure and Applied Chemistry (IUPAC) in the early 1960s to resolve a longstanding difference between two scales of the atomic mass unit. The term “atomic mass unit” (unit symbol: amu) has been used as a unit of mass defined as one-sixteenth the mass of a single atom 16O [m(16O)=16 amu] in physics and as one-sixteenth the isotope-averaged atomic mass (equivalent to the atomic weight) of oxygen [Ar(O)=16 amu] in chemistry.The Mass Spectrometry Society of Japan, 01 Dec. 2008, Journal of the Mass Spectrometry Society of Japan, 56(6) (6), 269 - 274, Japanese
The unit dalton (unit symbol: Da) is also a non-SI unit of mass defined as “1 Da=1 u,” and is accepted as a unit for use by the SI in the 8th edition of the SI brochure (2006). Therefore, both the unified atomic mass unit and dalton are authorized units for mass of ions and molecules.
It is a common mistake to use the deprecated term “atomic mass unit” and the deprecated unit symbol “amu” for the unit of mass defined as one-twelfth the mass of single atom 12C. The unit symbol “mmu,” meaning a millimass unit, is also an appropriate unit in SI. Instead of “mmu,” “mDa” or and “10-3 u” should be used.[Refereed]Introduction scientific journal - Dec. 2008, 化学, 63(12), 41, JapanesekDaは分子量の単位ではありません ~御用だ誤用だ! 「用語」の誤用、第8回Introduction scientific journal
- Nov. 2008, 化学, 63(11), 25, Japanese控えましょう! “mmu”を使うこと ~御用だ誤用だ! 「用語」の誤用、第7回Introduction scientific journal
- The Japanese word “masu” originates from the English word “mass.” It is occasionally used as an alias for units of mass and m/z. However, mass of molecules and ions should be expressed with the unified atomic mass unit (unit symbol: u) or dalton (unit symbol: Da). Furthermore, the m/z value indicated in the abscissa of mass spectra is dimensionless; therefore, it should not have any units.Lead, The Mass Spectrometry Society of Japan, 01 Oct. 2008, Journal of the Mass Spectrometry Society of Japan, 56(5) (5), 241 - 245, Japanese, Domestic magazineIntroduction scientific journal
- Sep. 2008, 化学, 63(9), 25, Japanese「amu」は、半世紀前に廃止された単位です ~御用だ誤用だ! 「用語」の誤用、第6回Introduction scientific journal
- Aug. 2008, 化学, 63(8), 17, Japanese使い分けましょう! 2種類の「精密質量」 ~御用だ誤用だ! 「用語」の誤用、第5回Introduction scientific journal
- Mass spectrometers separate ions according to each mass/charge value, which is not a dimensionless quantity. However, the m/z value indicated in the abscissa of mass spectra is defined as a dimensionless quantity and not a numerical value the same as the mass/charge value in kilograms/coulombs (kg/C) or in unified atomic mass units/coulombs (u/C). The numerical value of m/z converted from the mass/charge value depends on the unified atomic mass unit and the physical constant “elementary charge,” e that is also the atomic unit of charge. This conversion confuses many mass spectrometrists with regard to the abscissa labeling of mass spectra, e.g. the symbol “m/z” is considered as an abbreviation of the term “mass-to-charge ratio.”Lead, The Mass Spectrometry Society of Japan, 01 Aug. 2008, Journal of the Mass Spectrometry Society of Japan, 56(4) (4), 209 - 213, Japanese[Refereed]Introduction scientific journal
- Lead, 日本組織細胞化学会, 10 Jul. 2008, 組織細胞化学2008ーイメージングテクニックの入門とその応用ー, 75 - 85, Japanese, Domestic magazine細胞組織化学におけるプロテオミクス[Invited]Lecture materials
- Jul. 2008, 化学, 63(7), 44, Japanese控えましょう? 「娘イオン」を使うこと ~御用だ誤用だ! 「用語」の誤用、第4回Introduction scientific journal
- Some of mass spectrometrists refer to a term “mass number” as physical quantities of mass value and m/z value. However, the term “mass number” is defined as the sum of the total number of protons and neutrons in an atomic nucleus, atom, molecule, ion, or radical.The Mass Spectrometry Society of Japan, 01 Jun. 2008, Journal of the Mass Spectrometry Society of Japan, 56(3) (3), 173 - 178, Japanese[Refereed]Introduction scientific journal
- Jun. 2008, 化学, 63(6), 38, Japaneseこれからかわります! 「質量電荷比」の使い方 ~御用だ誤用だ! 「用語」の誤用、第3回Introduction scientific journal
- May 2008, 化学, 63(5), 40, Japaneseまちがえていませんか? 「分子イオン」の使い方 ~御用だ誤用だ! 「用語」の誤用、第2回Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Apr. 2008, Journal of the Mass Spectrometry Society of Japan, 56(2) (2), 55 - 56, Japanese[Refereed]Introduction scientific journal
- The Japanese word “mirimasu” originates from the English words “milli” and “mass.” It is normally used as an alias for “measured accurate mass” and “accurate mass measurement.” It causes confusions that “mirimasu” is also used as an alias for “high resolution mass spectrometry,” “high resolution mass spectrum (spectra),” and “mass spectrometer with high mass resolving power.” This nomenclature results from the fact that “high resolution” is confused with “high accuracy.” In addition to these interpretations, Japanese mass spectrometrists also use “mirimasu” as an alias for “one-thousandth of a unified atomic mass unit,” “one-thousandth of a dalton (mDa),” and “one-thousandth of an m/z unit.” This incorrect usage is due to a lack of understanding of the unit system of atomic mass and m/z on mass spectra. Therefore, “mirimasu” should not be used in Japanese, because it is ambiguous and involves various problems and misunderstandings.Lead, The Mass Spectrometry Society of Japan, 01 Apr. 2008, Journal of the Mass Spectrometry Society of Japan, 56(2) (2), 69 - 76, Japanese, Domestic magazineIntroduction scientific journal
- The Mass Spectrometry Society of Japan, 01 Apr. 2008, Journal of the Mass Spectrometry Society of Japan, 56(2) (2), 57 - 57, Japanese[Refereed]Introduction scientific journal
- Apr. 2008, 化学, 63(4), 48, Japaneseまちがえていませんか? 「質量数」の使い方 ~御用だ誤用だ! 「用語」の誤用、第1回Introduction scientific journal
- Linear mode, reflectron mode, and multi-turn are techniques for m/z analysis in time-of-flight mass spectrometry. Reflectron mode and multi-turn enable analysis to be performed with a higher mass resolving power than that attained with linear mode. In this commentary, starting from the basic principles of time-of-flight mass spectrometry in linear mode, the possible improvements in mass resolving power that can be made by reflectron mode and multi-turn techniques will be explained.The Mass Spectrometry Society of Japan, 01 Apr. 2008, Journal of the Mass Spectrometry Society of Japan, 56(2) (2), 49 - 54, Japanese[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2008, Journal of the Mass Spectrometry Society of Japan, 56(1) (1), 21 - 22, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- The terms “accurate mass” and “exact mass” are not synonymous in mass spectrometry. Accurate mass refers to the mass value of an ion or radical determined experimentally by mass spectrometry. On the other hand, exact mass refers to the mass value of a single ion, radical, or molecule calculated by summing the mass values of individual isotopes. To avoid confusion, “measured accurate mass” and “calculated exact mass” should be used in place of “accurate mass” and “exact mass,” respectively.Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2008, Journal of the Mass Spectrometry Society of Japan, 56(1) (1), 27 - 32, Japanese, Domestic magazineIntroduction scientific journal
- 2008, 日本薬理学雑誌, 132(3) (3)RalAはηPKCによるケラチノサイトの扁平化に必須である
- In terms related to mass spectrometry, “TIC” should be used as an abbreviation for “total ion current.” However, many mass spectrometrists use “TIC” as an abbreviation for “total ion chromatogram” while referring to “total ion current chromatogram,” which is incorrect. Another common misunderstanding related to abbreviations is the usage of “MCP” as an abbreviation for “multichannel plate,” which should be used for “microchannel plate.”Lead, The Mass Spectrometry Society of Japan, 01 Dec. 2007, Journal of the Mass Spectrometry Society of Japan, 55(6) (6), 381 - 388, Japanese, Domestic magazineIntroduction scientific journal
- Similar to a mass spectrometer, mass spectrograph is an instrument used to obtain mass spectra. In the mass spectrograph, ions with different m/z values are passed through a magnetic sector and dispersed in different trajectories similar to the dispersion of different wavelengths of light in a prism. The ions separated according to their m/z values are directed onto the same face and are simultaneously detected by a focal plane detector. This mass spectrum-measurement system is unique for instruments called as “mass spectrographs.” However, many mass spectrometrists refer to instruments that should be called “mass spectrometers” as “mass spectrographs.”Lead, The Mass Spectrometry Society of Japan, 01 Oct. 2007, Journal of the Mass Spectrometry Society of Japan, 55(5) (5), 353 - 361, Japanese, Domestic magazineIntroduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Aug. 2007, Journal of the Mass Spectrometry Society of Japan, 55(4) (4), 294 - 297, Japanese, Domestic magazineOthers
- The term “mass spectrometry” is usually abbreviated as “MS.” It is confusing that “MS” is also used as an abbreviation for “mass spectrometer,” “mass spectroscopy,” “mass spectrograph,” “mass spectrum (spectra),” and “mass separation.” “Masu” in Japanese is an ambiguous word and originates from “mass” in English or “Mass” in German. In addition to the meaning of mass, however, “masu” is used as an abbreviation for “mass spectrometry,” “mass spectrometer,” “unified atomic mass unit,” and “a quantity of m/z= 1” by Japanese mass spectrometrists. Because of the ambiguity in the usage of “MS” and “masu,” some inappropriate terms, such as “peptide MS fingerprinting” for “peptide mass fingerprinting” and “TOF-mass” for “time-of-flight mass spectrometer,” were used by Japanese mass spectrometrists.Lead, The Mass Spectrometry Society of Japan, 01 Aug. 2007, Journal of the Mass Spectrometry Society of Japan, 55(4) (4), 298 - 309, Japanese, Domestic magazineIntroduction scientific journal
- The term “restriction enzyme” is derived from the phenomenon of host-controlled restriction and modification in viral infection of bacteria, not from the ability of enzymes to recognize the specific target nucleotide sequence in the DNA and break the DNA chain. That is, the term “restriction enzyme” is not derived from the fact that the cleavage site is restricted. Bacteria initially resist infections by new bacteriophages, and this “restriction” of viral growth stems from endonucleases within the cells that destroy foreign DNA molecules from bacteriophages. Restriction enzymes are a kind of nuclease that catalyze hydrolysis of DNA strands and were discovered during investigations of the phenomenon of host-controlled restriction and modification of bacteriophages. They are not peptidases (proteases). However, it is a common mistake to use the term “restriction enzyme” for amino acid residue-specific endopeptidase such as trypsin.Lead, The Mass Spectrometry Society of Japan, 01 Jun. 2007, Journal of the Mass Spectrometry Society of Japan, 55(3) (3), 245 - 260, Japanese, Domestic magazineIntroduction scientific journal
- Ions are not organisms, and thus they do not proliferate by either sexual or asexual reproduction. They are hence incapable of being parents, children, or grandchildren. Therefore, the terms “parent ion,” “daughter ion,” and “granddaughter ion” are scientifically incorrect. In addition, mass spectrometrists should note that the terms “daughter ion” and “granddaughter ion” are gender-specific. (The terms “daughter nuclide” and “granddaughter nuclide” are also gender-specific.)Lead, The Mass Spectrometry Society of Japan, 01 Apr. 2007, Journal of the Mass Spectrometry Society of Japan, 55(2) (2), 99 - 115, Japanese, Domestic magazine
Therefore, the terms “parent ion” and “daughter ion” need to be replaced by “precursor ion” and “product ion,” respectively. Instead of the gender-specific terms “granddaughter ion” and “great-granddaughter ion,” the gender-neutral terms “second generation product ion” and “third generation product ion” should be used.Introduction scientific journal - Mass spectrometers separate ions according to each mass/charge value, which is not a dimensionless quantity. However, the m/z value indicated in the abscissa of mass spectra is defined as a dimensionless quantity and not a numerical value the same as the mass/charge value in kilograms/coulombs (kg/C). The numerical value of m/z converted from the mass/charge value depends on the unified atomic mass unit, u (or dalton, Da) and the physical constant “elementary charge,” e that is also the atomic unit of charge. This conversion confuses many mass spectrometrists with regard to the abscissa labeling of mass spectra. To avoid this confusion, a new unit, “thomson” (unit symbol, Th), was proposed, and defined as 1 Th=1 u/atomic charge=1 Da/atomic charge. However, this unit is not yet well known and has been deprecated.Lead, The Mass Spectrometry Society of Japan, 01 Feb. 2007, Journal of the Mass Spectrometry Society of Japan, 55(1) (1), 51 - 62, Japanese, Domestic magazineIntroduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Dec. 2006, Journal of the Mass Spectrometry Society of Japan, 54(6) (6), 255 - 255, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Dec. 2006, Journal of the Mass Spectrometry Society of Japan, 54(6) (6), 256 - 257, Japanese, International magazine[Refereed]Introduction scientific journal
- The unified atomic mass unit (unit symbol: u) is a non-SI unit of mass defined as one twelfth the mass of a single 12C atom in its ground state. This definition was agreed upon by both the International Union of Pure and Applied Physics and the International Union of Pure and Applied Chemistry in early 1960s to resolve a longstanding difference between two scales of atomic mass unit. The term “atomic mass unit” (unit symbol: amu) has been used to a unit of mass defined as one sixteenth the mass of a single atom 16O [m(16O)=16 amu] in physics, or as one sixteenth the isotope-averaged atomic mass (equivalent to the atomic weight) of oxygen [Ar(O)=16 amu] in chemistry.Corresponding, The Mass Spectrometry Society of Japan, 01 Dec. 2006, Journal of the Mass Spectrometry Society of Japan, 54(6) (6), 259 - 271, Japanese, International magazine
It is a common mistake to use the deprecated term “atomic mass unit” and the deprecated unit symbol “amu” for the unit of mass defined as one twelfth the mass of single atom 12C.Introduction scientific journal - Lead, The Mass Spectrometry Society of Japan, 01 Oct. 2006, Journal of the Mass Spectrometry Society of Japan, 54(5) (5), 219 - 227, Japanese, International magazineIntroduction scientific journal
- The Mass Spectrometry Society of Japan, 01 Oct. 2006, Journal of the Mass Spectrometry Society of Japan, 54(5) (5), 218 - 218, Japanese[Refereed]Introduction scientific journal
- Lead, The Mass Spectrometry Society of Japan, 01 Aug. 2006, Journal of the Mass Spectrometry Society of Japan, 54(4) (4), 175 - 182, Japanese, International magazineIntroduction scientific journal
- Lead, 日本質量分析学会, 01 Jun. 2006, Journal of the Mass Spectrometry Society of Japan, 54(3) (3), 119 - 126, Japanese, International magazineComments on Usage of the Terms "Sodium Adduct Ion" and "Protonated Molecular Ion"Introduction scientific journal
- Lead, 日本質量分析学会, 01 Apr. 2006, Journal of the Mass Spectrometry Society of Japan, 54(2) (2), 57 - 63, JapaneseComments on Usage of the Term "Molecular Ion"Introduction scientific journal
- Lead, 11 Feb. 2006, 医学のあゆみ, 216(6) (6), 477 - 478, JapaneseMammalian target of rapamycin (mTOR)[Invited]Introduction commerce magazine
- Lead, 日本質量分析学会, 01 Feb. 2006, Journal of the Mass Spectrometry Society of Japan, 54(1) (1), 33 - 37, Japanese, International magazineComments on Usage of the Term "Mass Number"Introduction scientific journal
- Lead, 日本質量分析学会, 01 Dec. 2005, 質量分析, 53(6) (6), 335 - 336, Japanese, Domestic magazineGood Medicine Is Bitter in the MouthOthers
- Lead, 日本質量分析学会, 01 Oct. 2005, 質量分析, 53(5) (5), 298 - 303, Japanese, Domestic magazineThe 53rd ASMS Conference (San Antonio,Texas) レポート FIESTA ASMS OLE!Meeting report
- Lead, 株式会社羊土社, 01 Jul. 2005, Experimental Medicine, 23(12) (12), 1939 - 1945, Japanese, Domestic magazineMammalian target of rapamycin complexes for cell growth comtrol devices[Invited]Introduction commerce magazine
- Lead, 日本質量分析学会, 01 Jun. 2005, 質量分析, 53(3) (3), 179 - 182, Japanese, Domestic magazine叡智に満ちたジャーナルへ ~編集委員長就任のご挨拶に代えて~Others
- JAPANESE SOCIETY FOR BACTERIOLOGY, 25 May 2005, Nippon Saikingaku Zasshi, 60(2) (2), 397 - 417, Japanese, Domestic magazine[Invited]Introduction scientific journal
- Lead, 東ソー株式会社科学計測事業部, 20 Jan. 2005, HLC MAILGRAM, 102(2005-1) (2005-1), 1 - 2, Japanese, Domestic magazineポストゲノム時代のLC/MS ④ MALDIでLC/MS[Invited]Introduction commerce magazine
- Lead, 東ソー株式会社科学計測事業部, 20 Aug. 2004, HLC MAILGRAM, 101(2004-4) (2004-4), 1 - 2, Japanese, Domestic magazineポストゲノム時代のLC/MS③ 象を飛ばしたエレクトロスプレーイオン化法[Invited]Introduction commerce magazine
- Lead, 日本質量分析学会, 01 Aug. 2004, 質量分析, 52(4) (4), 257 - 261, Japanese第52回ASMSコンファレンス(Nashville, Tennessee)レポート : キーワードはOPRY, ETD, FT-ICRそしてFLTMeeting report
- Lead, 東ソー株式会社科学計測事業部, 25 Jun. 2004, HLC MAILGRAM, 100(2004-3) (2004-3), 1 - 2, Japanese, Domestic magazineポストゲノム時代のLC/MS② ゲノムに直接支配されない生体分子群の解析[Invited]Introduction commerce magazine
- The progress in genome sequencing projects of a large number of organisms and the advance in mass spectrometry of protein analysis have been significant driving forces in the formation of the field proteomics. The advance in protein mass spectrometry includes development of computer algorithms that use mass spectrometric data to identify proteins in sequence databases. The computer algorithms for protein identification by correlation with sequence databases rely on the availability of constraining parameters that distinguish specific matches from all the other sequences in the database. They can be categorized into three strategies. One of strategies is called “peptide mass fingerprinting,” which is based upon correlating measured masses of peptides derived from digestion of proteins by a residue-specific protease with theoretically calculated peptide masses derived from proteins registered in sequence database. Two strategies for protein identification using tandem mass spectrometry (MS/MS) data are distinguished by demand for interpretation of product ion mass spectra. Product ion mass fingerprinting using uninterpreted MS/MS data of peptides is conceptually similar approach to peptide mass fingerprinting. SEQEUST® and MS/MS Ions Search in MASCOT® are the most widely used algorithms for protein identification by searching sequence database using uninterpreted product ion mass spectra. Another strategy using MS/MS data employs the search algorithm by using parameters, such as “peptide sequence tag,” found by manual inspection of product ion mass spectra.Lead, The Mass Spectrometry Society of Japan, 01 Jun. 2004, Journal of the Mass Spectrometry Society of Japan, 52(3) (3), 106 - 129, Japanese, Domestic magazine[Refereed]Introduction scientific journal
- Lead, 東ソー株式会社科学計測事業部, 15 Apr. 2004, HLC MAILGRAM, 99(2004-2) (2004-2), 1 - 2, Japanese, Domestic magazineポストゲノム時代のLC/MS① ポストゲノム時代を担うLC/MS[Invited]Introduction commerce magazine
- 秀潤社, Mar. 2004, 細胞工学, 23(3) (3), 340 - 348, Japanese, Domestic magazineラパマイシン標的タンパク質mTORシグナル伝達系[Invited]Introduction commerce magazine
- Raptor, a binding partner of target of rapamycinThe mammalian target of rapamycin (mTOR) controls cell growth in response to amino acids and growth factors, in part by regulating p70 S6 kinase alpha (p70 alpha) and eukaryotic initiation factor 4E binding protein 1 (4EBP1). Raptor (regulatory associated protein of mTOR) is a 150 kDa mTOR binding protein that is essential for TOR signaling in vivo and also binds 4EBP1 and p70alpha through their respective TOS (TOR signaling) motifs, a short conserved segment previously shown to be required for amino acid- and mTOR-dependent regulation of these substrates in vivo. Raptor appears to serve as an mTOR scaffold protein, the binding of which to the TOS motif of mTOR substrates is necessary for effective mTOR-catalyzed phosphorylation. Further understanding of regulation of the mTOR-raptor complex in response to the nutritional environment would require identification of the interplay between the mTOR-raptor complex and its upstream effectors such as the protein products of tumor suppressor gene tuberous sclerosis complexes 1 and 2, and the Ras-related small G protein Rheb.09 Jan. 2004, Biochemical and biophysical research communications, 313(2) (2), 437 - 441, English, International magazine[Refereed]Introduction scientific journal
- mTOR integrates amino acid- and energy-sensing pathwaysThe AMP-activated protein kinase (AMPK) exists as a heterotrimetric complex comprising a catalytic alpha subunit and non-catalytic beta and gamma subunits. Under conditions of hypoxia, exercise, ischemia, heat shock, and low glucose, AMPK is activated allosterically by rising cellular AMP and by phosphorylation of the catalytic alpha subunit. The mammalian target of rapamycin (mTOR) controls cellular functions in response to amino acids and growth factors. Recent reports including our study have demonstrated the possible interplay between mTOR and AMPK signaling pathways, supporting a model in which mitochondrial dysfunction caused by the mitochondrial inhibitors or ATP depletion inhibits activation of p70 S6 kinase alpha (p70alpha), a downstream effector of mTOR, by activating AMPK. Leucine may stimulate p70alpha phosphorylation via mTOR pathway, in part, by serving both as a mitochondrial fuel through oxidative carboxylation and an allosteric activation of glutamate dehydrogenase. This hypothesis may support an idea in which leucine modulates mTOR function, in part by regulating mitochondrial function and AMPK. Further understanding of the role of mTOR in coordinating amino acid- and energy-sensing pathways would provide new insights into relationship between nutrients and cellular functions.09 Jan. 2004, Biochemical and biophysical research communications, 313(2) (2), 443 - 446, English, International magazine[Refereed]Introduction scientific journal
- ANALYSIS OF RECOGNITION SITE FOR SRC-SPECIFIC MONOCLONAL ANTIBODY(Cell Biology and Morphology,Abstracts of papers presented at the 75^
Annual Meeting of the Zoological Society of Japan) : Zoological Society of Japan, 2004, Zoological science, 21(12) (12), 1285 - 1285, EnglishLead, 日本質量分析学会, 01 Oct. 2003, 質量分析, 51(5) (5), 559 - 561, Japanese第51回ASMSコンファレンス(Montréal, CANADA)レポート : SARS,ノーべル賞そしてエピジェネティクス[Refereed]Meeting reportメディカルレビュー社, Oct. 2003, 栄養 評価と治療, 20(5) (5), 478 - 482, Japanese, Domestic magazineアミノ酸と細胞内シグナル伝達-蛋白質合成を中心に[Invited]Introduction commerce magazineLead, 共立出版株式会社, 01 Aug. 2003, 蛋白質核酸酵素, 48(10) (10), 1378 - 1385, Japanese, Domestic magazine細胞成長を司る情報伝達システムの中央情報集積装置mTOR複合体[Refereed][Invited]Introduction commerce magazineLead, 医歯薬出版, 03 Aug. 2002, 医学のあゆみ, 202(5) (5), 325 - 330, Japanese暫定共通配列データベースを利用した新規タンパク質の同定[Invited]Introduction commerce magazineLead, 01 Oct. 2001, 質量分析, 49(5) (5), 215 - 216, Japanese, Domestic magazine第49回ASMS (Chicago, IL) レポート[Refereed]Meeting reportLead, Oct. 1998, 日本細菌学会関東支部ニュース, (32) (32), 7 - 7, Japanese, Domestic magazine海外会員便り[Invited]Introduction otherLead, (株)医薬ジャーナル社, May 1997, 化学療法の領域, 13(6) (6), 1155 - 1158, Japaneseベロ毒素吸着剤による大腸菌O157感染症治療法[Invited]Introduction commerce magazine(株)日本臨床社, Mar. 1997, 日本臨床, 55(3) (3), 693 - 699, JapaneseIntroduction commerce magazine(株)日本臨床社, Mar. 1997, 日本臨床, 55(3) (3), 751 - 757, JapaneseIntroduction commerce magazineLead, (株)文光堂, Feb. 1997, Quality Nursing, 3(2) (2), 191 - 195, Japanese, Domestic magazine[Invited]Introduction commerce magazineLead, National Institute of Health (Tokyo, JAPAN), 31 Jan. 1997, Japanese Journal of Medical Science and Biology, 49(5-6) (5-6), 256 - 257, English, International magazineAmino acid sequence of a peptide that inhibits human lymphocyte proliferation induced by the superantigen Yersinia pseudotuberculosis-derived mitogenIntroduction international proceedings31 Jan. 1997, Japanese Journal of Medical Science and Biology, 49(5-6) (5-6), 252 - 253, English, Domestic magazinePurification and characaterization of a novel variant of the superantigen Yersinia pseudotuberculosis-derived mitogenIntroduction international proceedings1996, 日本感染症学雑誌, 51(4) (4), 1037 - 1042, Japanese1996年夏、日本で多発した腸管出血性大腸菌O157感染症[Invited]Introduction scientific journal日水製薬(株), Jan. 1996, メディヤ サークル, 41(1) (1), 41 - 46, Japanese, Domestic magazine, Co-authored internationallyパルスフィールドゲル電気泳動によるYersinia pseudotuberculosisの分子疫学Introduction scientific journalLead, 国立予防衛生研究所, 25 Dec. 1995, Japanese Journal of Medical Science and Biology, 48(5-6) (5-6), 283 - 284, English, International magazineAmino Acid Sequences of the Precursor Protein and the Recombinant Toxin of a Novel Yersinia enterocolitica Heat-Stable Enterotoxin (Y-STc) that Incudes a 'Pro Region'-like Sequence in its Mature Toxin RegionIntroduction international proceedingsThe National Institute of Health (Tokyo), 25 Dec. 1995, Japanese Journal of Medical Science and Biology, 48(5-6) (5-6), 261 - 262, English, International magazineNucleotide sequence of the gene encoding a novel superantigen (YPM) produced by Yersinia pseudotuberculosis and the geographical heterogeneity in the prevalence of the geneIntroduction international proceedingsElsevier Science, 01 Dec. 1995, Kawasaki Disease: Proceedings of the 5th International Kawasaki Disease Symposium, Fukuoka, Japan, 193 - 199, English, International magazineEstablishment of a novel superantigen produced by Yersinia pseudotuberculosis and its association with systemic Kawasaki disease-like symptomsIntroduction international proceedingsMar. 1995, FASEB JOURNAL, 9(3) (3), A491 - A491, EnglishGENETIC-ANALYSIS OF A NOVEL SUPERANTIGEN PRODUCED BY YERSINIA-PSEUDOTUBERCULOSIS AND ITS EFFECT IN ACUTE-PHASE PATIENTSSummary international conferenceLead, The National Institute of Health (Tokyo), 25 Dec. 1994, Japanese Journal of Medical Science and Biology, 47(5-6) (5-6), 298 - 299, English, International magazinePurification and Protein Characterization of a Novel Superantigen Produced by a Yersinia pseudotuberculosis StrainIntroduction international proceedingsNational Institute of Health (Tokyo, JAPAN), 10 Mar. 1994, Japanese Journal of Medical Science and Biology, 46(5-6) (5-6), 238 - 239, English, International magazineIntroduction international proceedingsLead, National Institute of Health (Tokyo, JAPAN), 10 Mar. 1994, Japanese Journal of Medical Science and Biology, 46(5-6) (5-6), 236 - 237, English, International magazineIntroduction international proceedingsLast, Aug. 1992, Comparative Biochemistry and Physiology, 102B(4) (4), 679 - 690, English, International magazineThe relationship between amino acid sequences of sperm-activating peptides and the taxonomy of echinoids.[Refereed]Introduction scientific journalLead, Elsevier Science Publishers, 1992, Frontiers and New Horizons in Amino Asid Research, 315 - 320, English, International magazineA free o-bromophenylalanine, and o-, m-, p-phenylalanine- and bromohistidine-containing sperm-activating peptides in the extracellular matrix odf sea urchin eggsIntroduction international proceedingsLead, 1992, Peptide Chemstry 1991, 327 - 332, EnglishTandem mass spectrometry of a new SAP-IIB derivative isolated from the egg jelly of the sea urchin Stomosneustes variolarisSummary national conferenceLead, A. A. Balkema (Rotterdam), 1991, Biology of Echinodermata, 419 - 425, English, International magazineFurther structural stady of sperm-activating peptides isolated from the egg jelly of sea urchins, Tripneustes gratilla, Pseudoboletia maculata, Heterocentrotus mammillatus and Clypeaster japonicus, using fast atom bombardment mass spectrometryIntroduction international proceedingsLead, Protein Research Foundation, 1991, Peptide Chemistry 1990, 171 - 176, English, International magazine, Co-authored internationallyPrimary Structures of Bromophenylalanine-containing Sperm-activating PeptidesSummary national conferenceA. A. Balkema (Rotterdam), 1988, Echinoderm Biology, 213 - 218, English, International magazineTaxonomical significance of respiratory stimulation of sea urchin spermatozoa by egg associated substancesIntroduction international proceedings
■ Books And Other Publications- Editor, 一般社団法人日本質量分析学会, Mar. 2020, Japanese, ISBN: 9784902590906マススペクトロメトリー関係用語集(第4版)
- Contributor, 一般社団法人 日本規格協会, Mar. 2015, Japanese日本工業規格, 高速液体クロマトグラフィー質量分析通則 JIS K 0136:2015Others
- Contributor, 2.2 質量分析法によるシークエンシング, 丸善出版, Nov. 2012, Japanese, ISBN: 9784621086155タンパク質分析
- Contributor, オーム社, Oct. 2011, Japanese, ISBN: 9784274210914分析化学用語辞典
- Contributor, 第4章 質量分析法を利用したタンパク質同定法, 羊土社, Feb. 2011, Japanese, ISBN: 9784758101790改訂 タンパク質実験ハンドブック : 取り扱いの基礎から機能解析まで完全網羅!
- Joint editor, 日本質量分析学会, Jun. 2009, Japaneseマススペクトロメトリー関係用語集(第3版)Dictionary or encycropedia
- Contributor, 28. Signal transduction of egg fertilization : Focused proteomics on membrane/lipid rafts, Humana Press Inc., Totowa, NJ, Dec. 2005, 395-411, English, ISBN: 1588293629Xenopus protocols: cell biology and signal transduction (Methods in Molecular Biology, 322)Scholarly book
- Joint work, Kinase Activities Associated with mTOR, Springer, Aug. 2003, 271-282, English, ISBN: 354000534XTOR : target of rapamycin (Current Topics in Microbiology and Immunology, 279)Scholarly book
- Contributor, アミノ酸-mTOR-raptorシグナル伝達系の解明とインスリン作用, 株式会社 診断と治療社, Jun. 2003, 21-31, Japanese, ISBN: 4787813161糖尿病学2003Scholarly book
- Contributor, 質量分析法による配列未知蛋白質の同定:非哺乳動物モデル生物のプロテオーム解析, シーエムシー出版, Nov. 2002, 81-92, Japanese, ISBN: 4882317761プロテオミクスの最新技術 (シーエムシーBOOKS 669)Scholarly book
- Joint work, 2:インスリン作用の分子機構:4:mTORとインスリン作用, 金原出版, Mar. 2001, Japanese, ISBN: 4307510089分子糖尿病学の進歩 : 基礎から臨床まで(2001)
- Joint work, Chapter 30; Heat-stable enterotoxin of Vibrio and Yersinia species, Academic Press, Aug. 1999, 545-556, English, ISBN: 0120530759The Comprehensive Sourcebook of Bacterial Protein Toxins, Second EditionScholarly book
- Contributor, Early use of fosfomycin for Shiga toxin-producing Escherichia coli O157 infection reduces the risk of hemolytic uremic syndrome, American Society for Microbiology, Jul. 1998, 385-387, English, ISBN: 9781555811297Escherichia coli O157:H7 and other Shiga Toxin-Producing E. coli StrainsScholarly book
- Joint work, 6.タンパク質、6.3 修飾タンパク質, 東京化学同人, Apr. 1997, Japanese, ISBN: 480791331Xバイオロジカルマススペクトロメトリー (現代化学増刊 31)
- Joint work, Chapter 35:Purification and Characterization of a Novel Superantigen Produced by Yersinia pseudotuberclosis, Ios Pr Inc, Jan. 1997, English, Co-authored internationally, ISBN: 905199298XCytokines, Cholera and the GutScholarly book
- Joint work, Purification and gene cloning of a superantigen (YPM) produced by a patient strain of Yersinia pseudotuberculosis, pp. 331-333, S. Karger (Basel), Sep. 1995, English, ISBN: 9783805561389Contribution to Microbiology and Immunology: Volume 13; Yersiniosis: present and future: 6th International Symposium on Yersinia, Rome, September 26-28, 1994
- 第94回日本寄生虫学会大会, Mar. 2025, Japanese, 日本寄生虫学会, 大阪大学コンベンションセンター, Japan, Domestic conference熱帯熱マラリア原虫の生殖母体期におけるGAP45 の分子局在解析と相互 作用分子の探索Oral presentation
- 第34回泌尿器科分子・細胞研究会, Mar. 2025, Japanese, 泌尿器科分子・細胞研究会, なんばスカイオ コンベンションホール, Japan, Domestic conference前立腺癌細胞株のプロテアソーム阻害剤に対する薬剤耐性におけるPolo-like kinaseの役割Poster presentation
- 第53回質量分析講習会、基礎(A)コース「質量分析の基礎」, Dec. 2024, Japanese, 一般社団法人日本質量分析学会, Japan, Domestic conference質量分析用語[Invited]Public discourse
- 日本農芸化学会関西支部第533回講演会, Dec. 2024, Japanese, 公益財団法人日本農芸化学会, 神戸大学百年記念館(六甲台第2キャンパス), Japan, International conference植物におけるカテキン/ビタミンE受容体の相互作用蛋白質同定Oral presentation
- 第52回質量分析講習会、基礎(A)コース「質量分析の基礎」, Aug. 2024, Japanese, 一般社団法人日本質量分析学会, Japan質量分析用語[Invited]Public discourse
- 第72回質量分析総合討論会, Jun. 2024, English, 一般社団法人日本質量分析学会, つくば国際会議場, JapanIdentification of a Variant Protein of HSP70 Chaperone of Malaria Parasites (Plasmodium falciparum) by Mass Spectrometry and Database Searches using Extracted UniProtKB DatabasePoster presentation
- 第70回日本生化学会近畿支部例会, May 2024, Japanese, 日本生化学会近畿支部, 国立循環器病研究センターHSPB5を介した小胞体ストレス応答における小胞輸送のメカニズムの解明Oral presentation
- 第175回日本質量分析学会関西談話会, Mar. 2024, Japanese, 一般社団法人日本質量分析学会, 株式会社島津製作所関西支社、大阪梅田ツインタワーズ・サウス24階, Japan, Domestic conference質量分析への扉[Invited]Nominated symposium
- 第93回日本寄生虫学会大会, Mar. 2024, Japanese, 日本寄生虫学会, 順天堂大学本郷キャンパス, Japan, Domestic conference熱帯熱マラリア原虫の未成熟生殖母体期のSBP1はPfHSP70と相互作用するOral presentation
- 第51回質量分析講習会、基礎(A)コース「質量分析の基礎」, Nov. 2023, Japanese, 一般社団法人日本質量分析学会, 大阪大学産業科学研究所, Japan, Domestic conference質量分析用語[Invited]Public discourse
- 2023 International Joint Meeting of the 23rd International Conference on Cytochrome P450 and the 38th Annual Meeting of the Japanese Society for the Study of Xenobiotics [2023 ICCP450/JSSX], Sep. 2023, EnglishIdentification of bacterial binding proteins to perfluorooctanoic acidPoster presentation
- 第78 回日本寄生虫学会 西日本支部大会,, Sep. 2023, Japanese, 日本寄生虫学会, 愛媛大学 南加記念ホール・校友会館, Japan, Domestic conference熱帯熱マラリア原虫の生殖母体期における原虫タンパク質輸送の解析Oral presentation
- 第50回質量分析講習会、Aコース「質量分析の基礎」, May 2023, Japanese, 一般社団法人日本質量分析学会質量分析用語[Invited]Public discourse
- 第2回環境化学物質3学会合同大会, May 2023, Japanese, あわぎんホール(徳島県郷土文化会館), Japan, Domestic conference細菌由来のペルフルオロオクタン酸結合タンパク質の探索Poster presentation
- The 71st Annual Conference on the Mass Spectrometry Society of Japan, 2023, Osaka, May 2023, English, 日本質量分析学会, Japan, Domestic conferenceA Method for Efficient and Accurate Identification of Proteins of Malaria Parasites (Plasmodium falciparum) and Human, which are Prepared from Infected Red Blood Cells, by using Mass SpectrometryPoster presentation
- 第92回日本寄生虫学会大会, Mar. 2023, Japanese, 日本寄生虫学会, 金沢歌劇座(金沢市), Japan, International conference, Co-authored internationally熱帯熱マラリア原虫生殖母体期の原虫タンパク質輸送におけるSBP1 の機能解析Oral presentation
- 第49回質量分析講習会、Aコース「質量分析の基礎」, Nov. 2022, Japanese, 一般社団法人日本質量分析学会, Japan, Domestic conference質量分析用語[Invited]Public discourse
- 第77回日本寄生虫学会西日本支部大会大阪大会, Sep. 2022, Japanese熱帯熱マラリア原虫の生殖母体期におけるPTEX複合体の解析Oral presentation
- 第77回日本寄生虫学会西日本支部大会大阪大会, Sep. 2022, Japanese熱帯熱マラリア原虫生殖母体期のSBP1と相互作用するタンパク質の検索Oral presentation
- 第55回 日本原生生物学会大会, Sep. 2022, Japanese, 法政大学 小金井キャンパス, Japan, Domestic conference熱帯熱マラリア原虫生殖母体期のSBP1と相互作用するタンパク質の検索Oral presentation
- 第48回質量分析講習会、Aコース「質量分析の基礎」, Jul. 2022, Japanese, 一般社団法人日本質量分析学会, Japan質量分析用語[Invited]Public discourse
- The 70th Annual Conference on Mass Spectrometry, JAPAN, Jun. 2022, Japanese, 一般社団法人日本質量分析学会, 福岡国際会議場, Japan, Domestic conferenceThe actual condition of sequence databases of chicken Gallus gallus and a method for coping to identify allergen proteins derived from chicken egg yolk using mass spectrometry-based protein identificationPoster presentation
- 第91回日本寄生虫学会大会, May 2022, Japanese, とかちプラザ, Domestic conference熱帯熱マラリア原虫生殖母体期におけるPTEX複合体構成タンパク質の発現プロフ ァイル解析Poster presentation
- 第91回日本寄生虫学会大会, May 2022, Japanese, とかちプラザ, Domestic conference熱帯熱マラリア原虫生殖母体期におけるSBP1の機能解析Poster presentation
- 日本皮膚科学会第488回大阪地方会, Dec. 2021, Japanese, 庄田裕紀子(住友病院), Domestic conference卵黄による食物依存性運動誘発アナフィラキシーの1例Oral presentation
- Cell Bio 2021 Virtual-an Online ASCB|EMBO Meeting, Dec. 2021, English, The American Society for Cell BiologyPolo-like kinase 2 plays an essential role in cytoprotection in endoplasmic reticulum stress via phosphorylation of serine 19 in HSPB5Poster presentation
- Cell Bio 2021 Virtual-an Online ASCB|EMBO Meeting, Dec. 2021, English, The American Society for Cell BiologyPhosphorylation of HSPB1 regulates actin-myosin contraction in muscle cells via binding to the essential light chainPoster presentation
- 第47回質量分析講習会, Nov. 2021, Japanese, 一般社団法人日本質量分析学会, Japan, Domestic conference質量分析用語の正しい使い方(応用編)~用語の変遷をたどりながら~[Invited]Public discourse
- 第71回関西畜産学会大会, Oct. 2021, Japanese, 関西畜産学会, オンライン, Domestic conference黒毛和種牛の霜降り形質に関わるコラーゲンネットワークの役割についてOral presentation
- 日本農芸化学会2021年度西日本・中四国・関西支部合同大会, Sep. 2021, Japanese, 公益社団法人日本農芸化学会, Domestic conference黒毛和種牛の遺伝子発現プロファイルを用いた筋内脂肪のパスウェイ解析Oral presentation
- The 69th Annual Conference on Mass Spectrometry, May 2021, Japanese, 一般社団法人日本質量分析学会, オンライン, Domestic conferenceUsefulness of utilizing multiple spectrum libraries containing different CID product ion spectra derived from the same molecule in a library searchPoster presentation
- 日本食肉研究会第62回大会, Mar. 2021, Japanese, 神戸国際会議場&オンライン開催, Japan, Domestic conference黒毛和種の筋内脂肪パターン形成に関わる蛋白質の網羅的解析Poster presentation
- Cell Bio Virtual 2020, On Line ASCB | EMBO meeting, Dec. 2020, EnglishSmall heat shock protein suppresses apoptosis caused by endoplasmic reticulum stress in L6 myocytesPoster presentation
- Cell Bio 2020 Virtual-an Online ASCB | EMBO Meeting, Dec. 2020, EnglishProteomic analysis of senescence-like morphology induced by DNA damage in NIH3T3 cellsPoster presentation
- The 68th Annual Conference on Mass Spectrometry, May 2020, English, 一般社団法人日本質量分析学会, グランキューブ大阪(大阪府立国際会議場), Japan, Domestic conferenceIdentification of aminopropyl groups bound in the C-terminal region of branched-chain polyamine synthase (BpsA) by mass spectrometryPoster presentation
- The 68th Annual Conference on Mass Spectrometry, May 2020, Japanese, 一般社団法人日本質量分析学会, Domestic conferenceAnalysis of disease-related biomarker protein in urinePoster presentation
- 日本農芸化学会関西支部例会(第512回講演会), Feb. 2020, Japanese, 公益社団法人日本農芸化学会関西支部, 京都大学百周年時計台記念館 2階 国際交流ホール, Japan, Domestic conference筋細胞の小胞体ストレス応答におけるHSPB5の結合分子の探索と機能解析Oral presentation
- The American Society for Cell Biology 2019 ASCB/EMBO Meeting, Dec. 2019, English, The American Society for Cell Biology, Walter E. Washington Convention Center, United States, International conferenceIdentification of novel interacting proteins of small heat shock protein HSPB5 by using BioID2 methodPoster presentation
- 第42回日本分子生物学会年会, Dec. 2019, Japanese, マリンメッセ福岡, Japan, Domestic conferenceBioID法を用いたHSPB5の新規相互作用分子の探索Poster presentation
- 第27回北海道談話会・研究会、第16回質量分析技術者研究会, Oct. 2019, Japanese, 一般社団法人日本質量分析学会, 北海道大学創成科学研究棟, Japan, Domestic conference“TIC”, “MRM”, “magnetic sector”, “high resolution mass measurement”, “accurate mass measurement”の適切な用法と訳語(和文用語)Oral presentation
- The Annual Meeting of the Japan Society of Histochemistry and Cytochemistry, Sep. 2019, Japanese, Japan Society of Histochemistry and Cytochemistry, The Kobe Chamber of Commerce and Industry, Domestic conference低親和性ビオチン結合タンパク質Tamavidinを用いた新規ペプチド捕捉型BioID法の開発Poster presentation
- 第15回質量分析技術者研究会, Aug. 2019, Japanese, 一般社団法人日本質量分析学会, 大阪大学バイオテクノロジー国際交流棟(吹田市), Japan, Domestic conferenceモノアイソトピック質量と分子量,exact massとaccurate mass, m/zとはOral presentation
- 第46回BMSコンファレンス, Jul. 2019, Japanese, 日本質量分析学会, 札幌北広島クラッセホテル(北海道北広島市), Japan, Domestic conference問題を解きながら学ぶフラグメンテーション関連基礎用語[Invited]Public discourse
- 第67回質量分析総合討論会, May 2019, Japanese, 一般社団法人日本質量分析学会, つくば国際会議場 エポカルつくば, Japan, Domestic conference低親和性ビオチン結合タンパク質を用いたペプチド捕捉型BioID(近位依存性ビオチン標識)法による新規タンパク質間相互作用マッピング法Poster presentation
- 日本薬学会 第139回年会, Mar. 2019, Japanese, 公益社団法人日本薬学会, 幕張メッセ, Japan, Domestic conferenceバイオマーカー探索のための尿中タンパク質のプロテオーム解析Poster presentation
- 日本農芸化学会関西支部例会(第507回講演会), Feb. 2019, Japanese, 公益社団法人日本農芸会関西支部, 京都大学百周年時計台記念館, Japan, Domestic conferenceジアシルグリセロールキナーゼαの新規結合分子の探索Oral presentation
- 第24回質量分析学会北海道談話会・研究会、第150回関東談話会, Oct. 2018, Japanese, 一般社団法人日本質量分析学会, 北海道大学, Japan, Domestic conference化学修飾トリプシンスペクトルライブラリーを利用して 想定外断片の誤同定を防止する方法Oral presentation
- 第91回日本生化学会大会, Sep. 2018, Japanese, 公益社団法人日本生化学会, 国立京都国際会館, Japan, Domestic conferenceRhoA結合蛋白質として同定されたSTE20 like kinaseの筋細胞の肥大化における役割Poster presentation
- 第14回質量分析技術者研究会, Jul. 2018, Japanese, 質量分析技術者研究会, 奈良先端科学技術大学院大学先端科学技術研究科バイオサイエンス棟(生駒市), Japan, Domestic conferencekg定義改定についてOral presentation
- 第14回質量分析技術者研究会, Jul. 2018, Japanese, 質量分析技術者研究会, 奈良先端科学技術大学院大学先端科学技術研究科バイオサイエンス棟(生駒市), Japan, Domestic conference感度良く測定するためのコツは?Oral presentation
- 一般社団法人日本質量分析学会 第42回質量分析講習会, Jun. 2018, Japanese, 一般社団法人日本質量分析学会, 公益財団法人微生物化学研究会 微生物化学研究所, Japan, Domestic conference質量分析の基礎 ~測定原理からLC/MS~ 「全体のまとめと効果測定」[Invited]Public discourse
- 一般社団法人日本質量分析学会 第42回質量分析講習会, Jun. 2018, Japanese, 一般社団法人日本質量分析学会, 公益財団法人微生物化学研究会 微生物化学研究所, Domestic conference質量分析の基礎 ~測定原理からLC/MS~ 「1日目のまとめ」[Invited]Public discourse
- Mass Spectrometry and Proteomics 2018, May 2018, Japanese, 一般社団法人日本質量分析学会、日本プロオテオーム学会, Hotel Hankyu Expo Park, Japan, Domestic conferenceA novel and simple database search strategy to prevent false-positive identification by using a spectral library of unexpected peptides from chemically modified trypsinPoster presentation
- 第22回日本質量分析学会北海道談話会・研究会, Feb. 2018, Japanese, 旭川医科大学, Japan, Domestic conference大多数のプロテオミクス科学者が知らない化学修飾トリプシンの真実たち[Invited]Invited oral presentation
- The American Society for Cell Biology 2017 ASCB/IFCB Meeting, Dec. 2017, English, The American Society for Cell Biology, Philadelphia conventional center, Pennsylvania, International conferenceHSPB1 protein increases actomyosin ATPase activity of myofibrils fractionPoster presentation
- The American Society for Cell Biology 2017 ASCB/IFCB Meeting, Dec. 2017, English, The American Society for Cell Biology, Pennsylvania Convention Center, United States, International conference, Co-authored internationallyInvestigation of RhoA binding proteins using BioID systemPoster presentation
- 第21回質量分析学会北海道談話会・研究会, Oct. 2017, Japanese, 一般社団法人日本質量分析学会, 北海道大学, Japan, Domestic conference化学修飾トリプシンの知られざる素顔Oral presentation
- 第44回BMSコンファレンス, Jul. 2017, Japanese, 一般社団法人日本質量分析学会, 長浜ロイヤルホテル, Japan, Domestic conference現場の課題を一緒に考えてみませんか? 初心者がはまるリン酸化ペプチド分析の落とし穴[Invited]Nominated symposium
- The 44th Biological Mass Spectrometry Conference, Jul. 2017, Japanese, 日本質量分析学会, 長浜ロイヤルホテル(長浜市), Japan, Domestic conference問題を解きながら学ぶ質量分析用語[Invited]Public discourse
- The 65th Annual Conference on Mass Spectrometry, May 2017, Japanese, 一般社団法人日本質量分析学会, Tsukuba International Congress Center, Japan, Domestic conferenceStrategy for analysis of the splicing regulatory factors using high-resolution mass spectrometryPoster presentation
- The 65th Annual Conference on Mass Spectrometry, May 2017, Japanese, 一般社団法人日本質量分析学会, Tsukuba International Congress Center, Japan, Domestic conferenceInconvenient truths of chemically modified trypsinPoster presentation
- The American Society for Cell Biology 2016 ASCB/IFCB Meeting, Dec. 2016, English, Moscone Center San Francisco, California, United States, International conference, Co-authored internationallyIdentification of novel RhoA binding proteins by using BioID systemPoster presentation
- The American Society for Cell Biology 2016 ASCB/IFCB Meeting, Dec. 2016, English, Moscone Center San Francisco, United States, International conferenceIdentification of novel HSPB1 binding proteins in skeletal musclePoster presentation
- 第39回日本分子生物学会年会, Dec. 2016, Japanese, パシフィコ横浜, Japan, Domestic conferenceIdentification of novel RhoA binding protein by usinBioID systemPoster presentation
- 第18回日本質量分析学会北海道談話会・研究会, Oct. 2016, Japanese, 一般社団法人日本質量分析学会, 北海道大学創成科学研究棟(札幌市), Japan, Domestic conference今さら聞けない質量分析用語の疑問点Oral presentation
- 日本農芸化学会2016年度関西支部講演会(第496回講演会), Sep. 2016, Japanese, 公益社団法人日本農芸化学会関西支部, 滋賀県立大学(滋賀県彦根市八坂町2500), Japan, Domestic conference骨格筋におけるHSPB1結合蛋白質の探索とそのアクトミオシンの ATPase活性に与える影響Oral presentation
- 第63回日本生化学会近畿支部例会, May 2016, Japanese, 公益社団法人日本生化学会近畿支部, 神戸薬科大学, Japan, Domestic conference筋肉の増加減退に関わるRhoAの機能解析と相互作用分子の探索Oral presentation
- 第64回質量分析総合討論会, May 2016, Japanese, 一般社団法人日本質量分析学会, ホテル阪急エキスポパーク, Japan, Domestic conference質量分析法を用いたスプライシング制御機構解明へのアプローチPoster presentation
- 日本薬学会 第136年会, Mar. 2016, Japanese, 公益社団法人日本薬学会, パシフィコ横浜, Japan, Domestic conference質量分析法を利用したRNA結合蛋白質の解析Poster presentation
- 第38回日本分子生物学会年会、第88回日本生化学会合同大会, Dec. 2015, Japanese, 神戸国際展示場, Japan, Domestic conference質量分析法を利用したスプライシング制御因子の解析Poster presentation
- 第65回日本薬学会近畿支部大会, Oct. 2015, Japanese, 公益社団法人日本薬学会関西支部, 大阪大谷大学, Japan, Domestic conferenceRNAスプライシングを制御する蛋白質の分析Oral presentation
- SciX 2015, Sep. 2015, English, FACSS (The Federation of Analytical Chemistry and Spectroscopy Societies), Rhode Island Convention Center, Providence, RI, United States, International conferenceIdentification of the splicing regulatory factors using mass spectrometryPoster presentation
- 第42回BMSコンファレンス, Jul. 2015, Japanese, 一般社団法人日本質量分析学会, 岐阜グランドホテル, Japan, Domestic conferenceRNA結合蛋白質の解析Poster presentation
- 第42回BMSコンファレンス, Jul. 2015, Japanese, 一般社団法人日本質量分析学会, 岐阜グランドホテル(岐阜市), Japan, Domestic conference質量分析用語基礎講座[Invited]Public discourse
- 第63回質量分析総合討論会, Jun. 2015, Japanese, 一般社団法人日本質量分析学会, つくば国際会議場(つくば市), Japan, Domestic conferencenanoLC/ESI電場型フーリエ変換質量分析法による、封入体からのタンパク質可溶化試薬TAPS-sulfonateを用いる大腸菌リコンビナントヒトインスリン精製工程の評価Poster presentation
- 第63回質量分析総合討論会, Jun. 2015, Japanese, 一般社団法人日本質量分析学会, つくば国際会議場(つくば市), Japan, Domestic conferenceエクソン認識を制御するRNA結合蛋白質解析法の構築Oral presentation
- 日本薬学会第135年会, Mar. 2015, Japanese, 公益社団法人日本薬学会, デザイン・クリエイティブセンター神戸, Japan, Domestic conference高分解能LC-MS/MSを用いるRNA結合蛋白質hnRNPA1の同定Poster presentation
- 第87回日本生化学会大会, Oct. 2014, Japanese, 公益社団法人日本生化学会, 国立京都国際会館, Japan, Domestic conference筋細胞におけるHSPB1の結合分子の探索とその機能解析Poster presentation
- 第37回日本神経科学大会, Sep. 2014, Japanese, 日本神経科学会, 横浜, Domestic conferencePKC KO Parkinsonian syndrome model:The role of PIX phosphorylation at Ser340 and Ser583 in dopamine release.Poster presentation
- Society for Neuroscience 2014, Sep. 2014, English, Society for Neuroscience, Washington D.C., USA, International conferenceAnalysis of PKC substrates in nigro-striatum system:The role of bPIX phosphorylation for dopamine release.Oral presentation
- 第41回BMSコンファレンス, Jul. 2014, Japanese, 日本質量分析学会, 能登ロイヤルホテル(石川県志賀町), Japan, Domestic conferenceIUPAC質量分析用語集(2013勧告)におけるMSSJ用語集第3版(2009)からの主要な変更点とその注意点Poster presentation
- 第62回質量分析総合討論会, May 2014, Japanese, 日本質量分析学会, ホテル阪急エキスポパーク, Japan, Domestic conferenceMSSJ用語集(第3版)とIUPAC質量分析用語集2013との差分・増分について[Invited]Nominated symposium
- 第55回日本神経学会学術大会, May 2014, Japanese, 日本神経学会, 福岡, Domestic conferencePKCノックアウトパーキンソン症候群モデル:bPIXリン酸化のドパミン遊離での役割Poster presentation
- 第40回BMSコンファレンス, Jul. 2013, Japanese, 日本質量分析学会, シーガイアコンベンションセンター(宮崎市), Japan, Domestic conferenceマススペクトルデータ表記法[Invited]Public discourse
- 第33回質量分析講習会基礎コース, May 2013, Japanese, 日本質量分析学会, 千里ライフサイエンスサンタ―, Japan, Domestic conference基礎用語[Invited]Public discourse
- 第35回日本分子生物学会年会, Dec. 2012, Japanese, 福岡, Domestic conferenceThe Functional Analysis of the Modifications of the DNA Damage Recognition Protein DDB2(2W5II-6)Keynote oral presentation
- 第35回日本分子生物学会年会, Dec. 2012, Japanese, 福岡, Domestic conferenceExploration of Novel Regulatory Factors in Mammalian Nucleotide Excision Repair (1ST3-018)Poster presentation
- 第32回質量分析講習会基礎コース, Nov. 2012, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference基礎用語[Invited]Public discourse
- The 8th 3R Symposium (International Symposium on DNA Replication, Recombination and Repair), Nov. 2012, English, Awaji, International conferenceFunctional studies on ubiquitylation of the DNA damage recognition protein DDB2Public symposium
- 第6回日本質量分析学会北海道談話会・研究会, Oct. 2012, Japanese, 日本質量分析学会, 北海道大学創成研究棟, Japanデータベース未登録タンパク質をMASCOT検索によって同定するための変法 ~鶏肉(かしわ)由来タンパク質をモデルとして~Oral presentation
- International Mass Spectrometry Conference (IMSC) 2012特別企画・質量分析の基礎と最先端(特別勉強会)~プロダクトイオンスペクトルの解釈から薬物動態質量分析へ, Sep. 2012, Japanese, 国立京都国際会館(京都市), International conferenceマススペクトルを正しく理解するための質量分析用語の基礎[Invited]Public discourse
- 22th IUBMB & 37th FEBS, Sep. 2012, English, Spain, International conferenceRole of PKCalpha-mediated cofilin phosphorylation in the degranulation from RBL-2H3 mast cells.Poster presentation
- 第31回質量分析講習会, Jun. 2012, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference基礎用語[Invited]Public discourse
- 第121回日本薬理学会近畿部会, Mar. 2012, Japanese, 日本薬理学会, 徳島, Domestic conference黒質線条体系におけるPKCgammaの基質の解析Oral presentation
- 第30回質量分析講習会, Dec. 2011, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference基礎用語[Invited]Public discourse
- 質量分析講習会アドバンストコース, Nov. 2011, Japanese, 日本質量分析学会, 日本化学会・化学会館, Japan, Domestic conference新しいMSのパワーを知る、プロテオーム関連MS、Q-TOF-MS[Invited]Public discourse
- 第84回日本生化学会, Sep. 2011, Japanese, 日本生化学会, 京都, Domestic conferenceNovel phosphorylation site(s) of cofilin by PKCalpha contributes toproper termination of histamine releaseOral presentation
- 第33回日本分子生物学会年会・第83回日本生化学会年会 合同大会, Dec. 2010, Japanese, 特定非営利活動法人日本分子生物学会・社団法人日本生化学会, 神戸ポートピアホテル、神戸国際会議場、神戸国際展示場, Domestic conference脊髄小脳失調症14型 (SCA14)の原因となる変異γPKCはheat shock cognate protein 70 (Hsc70)と結合し、そのリソソームへのトランスロケーションを抑制するOral presentation
- 第6回質量分析技術者近畿ブロック研究会, Jul. 2010, Japanese, 質量分析技術者近畿ブロック研究会, 京都大学大学院薬学研究科本館, Japan, Domestic conferenceいけないマススペクトロメトリー[Invited]Invited oral presentation
- サーモフィッシャーサイエンティフィック株式会社質量分析計ユーザーズフォーラム2010(東京会場), Jul. 2010, Japanese, サーモフィッシャーサイエンティフィック株式会社, ホテルラフォーレ東京(品川区), Japan, Domestic conference質量分析用語がわかる ~イケナイ質量分析用語~[Invited]Public discourse
- サーモフィッシャーサイエンティフィック株式会社質量分析計ユーザーズフォーラム2010(大阪会場), Jul. 2010, Japanese, サーモフィッシャーサイエンティフィック株式会社, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference質量分析用語がわかる ~イケナイ質量分析用語~[Invited]Public discourse
- 第37回BMSコンファレンス, Jul. 2010, Japanese, 日本質量分析学会, 沖縄残波岬ロイヤルホテル, Japan, Domestic conference質量分析基礎用語[Invited]Public discourse
- 第8回北海道質量分析研究会、日本質量分析学会北海道地区研究・講演会, Sep. 2009, Japanese, 北海道質量分析研究会、日本質量分析学会, 北海道大学薬学部, Japan, Domestic conference質量分析関連用語IUPACおよびMSSJ新勧告[Invited]Invited oral presentation
- 第25回質量分析講習会基礎コース, Jun. 2009, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference質量分析基礎用語[Invited]Public discourse
- 第57回質量分析総合討論会, May 2009, Japanese, 日本質量分析学会, 大阪国際交流センター(大阪市), Japan, Domestic conferenceマススペクトルの基礎用語[Invited]Nominated symposium
- 第24回質量分析講習会基礎コース, Nov. 2008, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference質量分析基礎用語[Invited]Public discourse
- 第24回質量分析講習会, Nov. 2008, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(大阪府豊中市), Domestic conferenceマススペクトルの読み方[Invited]Invited oral presentation
- 第33回組織細胞化学講習会, Aug. 2008, Japanese, 日本組織細胞化学会, 神戸国際会議場, Japan, Domestic conference組織細胞化学におけるプロテオミクスInvited oral presentation
- The 35th Biological Mass Spectrometry Conference, Jul. 2008, Japanese, 日本質量分析学会, 裏磐梯ロイヤルホテル, Japan, Domestic conference間違いやすい質量分析の基礎用語Poster presentation
- 第23回質量分析講習会, Jun. 2008, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conferenceマススペクトルの読み方 1 ~用語解説を中心に~[Invited]Public discourse
- 第23回質量分析講習会, Jun. 2008, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(大阪府豊中市), Domestic conferenceマススペクトルの読み方 3[Invited]Invited oral presentation
- 第113回日本薬理学会近畿部会, Jun. 2008, Japanese, 岡山, Domestic conferenceRalAはeta PKCによるケラチノサイトの扁平化に必須であるOral presentation
- 第56回質量分析総合討論会, May 2008, Japanese, 日本質量分析学会, つくば国際会議場エポカル, Domestic conference質量分析基礎用語・IUPAC新勧告のポイント[Invited]Nominated symposium
- The 56th Annual Conference on Mass Spectrometry, May 2008, Japanese, 日本質量分析学会, International Congress Center Epochal Tsukuba, Japan, Domestic conferenceEssential terms of mass spectrometry that need to be discussed[Invited]Nominated symposium
- The 56th Annual Conference on Mass Spectrometry, May 2008, Japanese, 日本質量分析学会, International Congress Center Epochal Tsukuba, Domestic conferenceMass-Spectrometry-based Protein Identification by Correlation with Sequence Databases and Mass Spectrometric Fragmentation[Invited]Invited oral presentation
- 第22回質量分析講習会, Nov. 2007, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(大阪府豊中市), Domestic conferenceマススペクトルの読み方 3[Invited]Invited oral presentation
- 第22回質量分析講習会, Nov. 2007, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Domestic conferenceマススペクトルの読み方 1 ~用語解説を中心に~[Invited]Public discourse
- The 34th Biological Mass Spectrometry Conference, Jul. 2007, Japanese, 日本質量分析学会, 鳥羽シーサイドホテル, Japan, Domestic conference用語を通して学ぶ質量分析・基礎の基礎 ~目から鱗のマススペクトロメトリー@BMSコンファレンス~[Invited]Public discourse
- 田中耕一記念質量分析研究所社内セミナー, Jun. 2007, Japanese, 株式会社島津製作所, 株式会社島津製作所(京都市), Japan, Domestic conference質量分析用語の正しい使い方[Invited]Public discourse
- 第54回質量分析総合討論会, May 2007, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference質量分析用語の諸課題[Invited]Nominated symposium
- The 55h Annual Conference on Mass Spectrometry, May 2007, Japanese, 日本質量分析学会, 広島国際会議場, Domestic conferenceCurrent Problems of the Terms relating to Mass Spectrometry[Invited]Nominated symposium
- MBSJ Forum 2006, Molecular Biology -the Next Decade-conference & Scientific, Dec. 2006, English, 名古屋国際会議場, International conferenceIdentification of TBC7, a TBC (Tre-2/Bub2/Cdc16) domain protein, as a novel component of the TSC1-TSC2 tumor suppressors.Oral presentation
- The 4th JHUPO and the 2nd JSCP Joint Conference, Jul. 2006, Japanese, 日本ヒトプロテオーム機構第4回大会、, 東京都新宿区、京王プラザホテル, Japan, Domestic conferencePhosphoproteome Analysis by LC/MSn with Linear Ion Trap Mass SpectrometerOral presentation
- 第33回BMSコンファレンス, Jul. 2006, Japanese, 日本質量分析学会, 大津プリンスホテル, Japan, Domestic conference質量スペクトルの読み方[Invited]Public discourse
- 神戸大学21世紀COEプログラム拠点「蛋白質のシグナル伝達機能」拠点内技術講習会, Jun. 2006, Japanese, 神戸大学21世紀COEプログラム拠点「蛋白質のシグナル伝達機能」, 神戸大学遺伝子実験センター, Japan, International conferenceマススペクトルデータを用いた配列データベース検索による蛋白質同定法Public discourse
- 第54回質量分析総合討論会, May 2006, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conferenceA database search protocol for the detection of Ser/Thr phosphorylation on proteins by LC/MSn with linear ion trap mass spectrometerPoster presentation
- 第54回質量分析総合討論会, May 2006, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター(豊中市), Japan, Domestic conference質量分析関連用語の課題の克服とジャーナル編集[Invited]Nominated symposium
- Cold Spring Harbor Conference on PTEN Pathways, Mar. 2006, English, New York, International conferenceTOS and RAIP motifs of the translational regulator protein 4E-BP1 play different roles for the association with raptor and phosphorylation by mTOR in the regulation of cell sizeOral presentation
- 第28回日本分子生物学会年会(福岡), Dec. 2005, Japanese, 日本分子生物学会, 福岡Yahoo! JAPANドーム, Japan, Domestic conferencemTOR による4EBP1のリン酸化を介した分子間相互作用と細胞サイズの制御Poster presentation
- 第28回日本分子生物学会年会(福岡), Dec. 2005, Japanese, 日本分子生物学会, 福岡Yahoo! JAPANドーム, Japan, Domestic conferenceNeurospora crassaミトコンドリアリボソーム蛋白質遺伝子の同定と進化的解析Poster presentation
- Thermo Electron Users' Forum 2005 製薬・ライフサイエンスLC/MSユーザーズフォーラム(大阪会場), Nov. 2005, Japanese, サーモエレクトロン株式会社, 千里ライフサイエンスセンター新しい「切り口」で攻めるプロテオーム解析Public discourse
- 第78回日本生化学会大会(神戸), Oct. 2005, English, 神戸国際会議場、神戸国際展示場、神戸ポートピアホテル, Japan, Domestic conferenceBiochemical and morphological analysis of the interaction of oligodendrocyte membrane rafts with actin filamentsPoster presentation
- 第78回日本生化学会大会(神戸), Oct. 2005, English, 神戸, Japan, Domestic conferenceSuppression of the mTOR-raptor signaling pathway by the inhibitor of heat shock protein 90 geldanamycin.Oral presentation
- 第23回日本細菌学会技術講習会, Sep. 2005, Japanese, 日本細菌学会, 千里ライフサイエンスセンター、島津製作所本社, Japan, Domestic conference質量分析による蛋白質同定法[Invited]Public discourse
- 第39回千里ライフサイエンスセンター技術講習会「プロテオミクス技術講習会、MALDI、ESI、MS/MS、ナノLC、データ解析」, Jul. 2005, Japanese, 財団法人千里ライフサイエンス振興財団, 千里ライフサイエンスセンター, Japan, Domestic conferenceマススペクトルデータを利用したデータベース検索による蛋白質同定の基礎[Invited]Public discourse
- 質量分析講習会基礎コース, Jun. 2005, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター, Japan, Domestic conferenceマススペクトルの読み方2[Invited]Public discourse
- 第52回日本生化学会近畿支部例会, May 2005, Japanese, Kobe, Domestic conferencemTORシグナリングに対する分子シャペロンHsp90の寄与Oral presentation
- 第53回質量分析総合討論会(さいたま), May 2005, Japanese, 日本質量分析学会, 大宮ソニックシティ, Japan, Domestic conferenceナノエレクトロスプレーイオン化四重極飛行時間型タンデム質量分析法を用いた分子量6,000を超える高分子量ペプチドのアミノ酸配列解析:in-house配列データベース検索エンジンの新たな利用法Poster presentation
- 山口大学大学院医学研究科大学院セミナー, May 2005, Japanese, 山口大学大学院医学研究科, 山口大学大学院医学研究科, Japan, Domestic conference質量分析法による新規蛋白質の探索とその機能解析[Invited]Public discourse
- 第27回日本分子生物学会年会, Dec. 2004, 日本分子生物学会, 神戸ポートアイランド, Domestic conferenceMolecular Identification and Immunochemical Characterization of Src Tyrosine Kinase Xenopus EggsPoster presentation
- 第27回日本分子生物学会年会, Dec. 2004, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferencemTOR複合体を構成するWDリピート蛋白質mLST8の機能解析Poster presentation
- 第27回日本分子生物学会年会, Dec. 2004, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferencemTORを中枢としたアミノ酸情報感知伝達/細胞成長制御システムを担う分子探索Poster presentation
- The 27th Annual Meeting of the Molecular Biology Society of Japan, Dec. 2004, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferenceThe functions and phylogenetic correspondence of mitochondrial ribosomal proteins of Neurospora crassaPoster presentation
- 第27回日本分子生物学会年会, Dec. 2004, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferencemTORを介し細胞機能を制御するシグナル伝達系の研究[Invited]Nominated symposium
- 質量分析講習会基礎コース, Nov. 2004, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター, Japan, Domestic conferenceマススペクトルの読み方2[Invited]Public discourse
- ジャスコインタナショナルプロテオミクスセミナー2004(大阪会場), Nov. 2004, Japanese, ジャスコインタナショナル株式会社, 大阪国際会議場「グランキューブ大阪」エレクトロスプレーイオン化-四重極-飛行時間型質量分析計の魅力[Invited]Public discourse
- ジャスコインタナショナルプロテオミクスセミナー2004(東京会場), Nov. 2004, Japanese, ジャスコインタナショナル株式会社, 主婦会館「プラザエフ」, Japan, Domestic conferenceエレクトロスプレーイオン化-四重極-飛行時間型質量分析計の魅力[Invited]Public discourse
- 第77回日本生化学会大会, Oct. 2004, Japanese, 日本生化学会, パシフィコ横浜Molecular identification of uroplakin III as a raft protein that is tyrosine-phosphorylated upon fertilization of Xenopus eggsNominated symposium
- 第77回日本生化学会, Oct. 2004, English, 日本生化学会, パシフィコ横浜, Domestic conferenceIdentification and Functional Analysis of Phosphorylation sites of a Novel Protein Raptor which is an Essential Scaffold Protein for mTOR SignalingNominated symposium
- 第77回日本生化学会大会, Oct. 2004, Japanese, 日本生化学会, パシフィコ横浜, Japan, Domestic conferenceBinding between 4EBP1 and raptor is regulated by mTOR phosphorylation of 4EBP1Nominated symposium
- 第6回RNAミーティング/第6回日本RNA学会年会(熊本), Aug. 2004, Japanese, 日本RNA学会, 熊本テルサ, Domestic conferenceRNA翻訳制御スイッチとして働くラパマイシン標的蛋白mTORシグナルの研究
- Gordon Research Conference "Second Messengers and Protein Phosphorylation", Jun. 2004, English, New Hampshire, United States, International conference, Co-authored internationallyDissociation of raptor from mTOR is a mechanism of rapamaycin-induced inhibition of mTOR functionPoster presentation
- 質量分析講習会応用コース1「プロテインマススペクトロメトリー」, Jun. 2004, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター, Japan, Domestic conference配列データベース検索による蛋白質の同定[Invited]Public discourse
- 第52回質量分析総合討論会, Jun. 2004, Japanese, 日本質量分析学会, 名古屋市工業研究所, Japan, Domestic conferenceESTコンセンサス配列データベースを用いた新規チロシンリン酸化蛋白質の同定Oral presentation
- 第57回日本細胞生物学会大会, May 2004Dissociation of raptor from mTOR is a mechanism of rapamycin-induced inhibition of mTOR function
- 52nd ASMS Conference on Mass Spectrometry and Allied Topics, May 2004, English, Gayload Ppryland Hotel, Nashville, TN, United States, International conferenceMass Spectrometric Identification of a Novel Egg Plasma Membrane Rafts-Associated Protein that is Tyrosine-Phosphorylated upon FertilizationPoster presentation
- Kobe University The 21st Century COE Program "Signaling Mechanisms by Protein Modification Reactions", The 1st Iternational Meeting "Conference on Lipid Messenger Signaling", Jan. 2004, English, Kobe University, Japan, International conferenceThe mammalian target of rapamycin (mTOR) partner, raptor binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif.Oral presentation
- The 8th Korea-Japan Cancer Research Workshop, Dec. 2003, English, Okinawa Miyako Hotel (Naha, Okinawa, Japan), International conferenceMass spectrometric identification and functional analysis of novel protein components of mTOR (mammalian target of rapamicin ) complex[Invited]Poster presentation
- 第26回日本分子生物学会年会(神戸), Dec. 2003, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferenceRapamicinによるmTOR (mammalian target of rapamysin) シグナル抑制機構Oral presentation
- 第26回日本分子生物学会年会(神戸), Dec. 2003, English, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferenceMolecular identification of Xenopus egg uroplakin III that localizes to rafts and is tyrosine-phosphorylated upon fertilization.Oral presentation
- 第26回日本分子生物学会年会(神戸), Dec. 2003, Japanese, 日本分子生物学会, 神戸ポートアイランド, Japan, Domestic conferenceミトコンドリアリボソーム蛋白質遺伝子の構造と機能:比較的解析と進化的意義Poster presentation
- The New Frontier of RNA (RNA 2003 Kyoto), Nov. 2003, English, International conferenceThe mammalian target of rapamycin (mTOR) partner, raptor binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif
- 質量分析講習会応用コース1「プロテインマススペクトロメトリー」, Nov. 2003, Japanese, 日本質量分析学会, 千里ライフサイエンスセンター, Japan, Domestic conference配列データベース検索による蛋白質の同定[Invited]Public discourse
- Neuroscience 2003, 33rd Annual Meeting of Society for Neuroscience, Nov. 2003, EnglishDirect binding and phosphorylation of two purkinje cell-enriched kinese, DGKγ and γPKC, regulate their spatio-tenporal activities
- 第76回日本生化学会大会, Oct. 2003, English, 日本生化学会, パシフィコ横浜, Japan, Domestic conferenceCellular signaling through an mTOR- containing complex.[Invited]Nominated symposium
- 第76回日本生化学会大会, Oct. 2003, English, 日本生化学会, パシフィコ横浜, Japan, Domestic conferenceFunctional and Moleculer Interaction between DGKγ and γPKCPoster presentation
- 第76回日本生化学会大会, Oct. 2003, English, 日本生化学会, パシフィコ横浜, Japan, Domestic conferenceThe seven WD-repeats protein Gable is one of components of mTOR complex.Poster presentation
- 第76回日本生化学会大会, Oct. 2003, English, 日本生化学会, パシフィコ横浜, Japan, Domestic conferencemTOR binding protein, raptor, binds to mTOR substrates via TOS motif.Poster presentation
- 神戸大学21世紀COEプログラム拠点「蛋白質のシグナル伝達機能」拠点内技術講習会, Oct. 2003, Japanese, 神戸大学21世紀COEプログラム拠点「蛋白質のシグナル伝達機能」, 神戸大学バイオシグナル研究センター, Japan, International conferenceMALDI-TOF-MSとMascotを用いたペプチドマスフィンガープリンティング(PMF)法による蛋白質同定法Public discourse
- 第30回BMSコンファレンス, Jul. 2003, Japanese, 日本質量分析学会, 淡路夢舞台国際会議場, Japan, Domestic conference質量分析法と配列データベースを利用した蛋白質の同定[Invited]Public discourse
- 第3回日本蛋白質化学会年会, Jun. 2003, Japanese, 日本蛋白質化学会, 札幌コンベンションセンター(札幌市), Domestic conference質量分析を用いたアミロイド線維の最終形態を決定付ける中間体のキャラクタリゼーションPoster presentation
- 第39回日本肝臓学会総会サテライトシンポジウム第5回AJINOMOTO Award受賞記念講演会, May 2003, Japanese, 日本肝臓学会, 福岡国際会議場, Japan, Domestic conference分岐鎖アミノ酸シグナル伝達系の中枢分子mTORに結合し、その活性を制御する新規分子raptorの同定と機能解析[Invited]Nominated symposium
- 第51回質量分析総合討論会, May 2003, Japanese, 日本質量分析学会, 独立行政法人産業技術総合研究所(つくば本部・つくばセンター), Japan, Domestic conference質量分析法によるアミロイド線維形成における構造単位の同定Oral presentation
- 第4回PIKPK研究会, Apr. 2003, Japanese, 神戸大学, Japan, Domestic conferencemTOR結合分子raptorはTOSmtifを介してmTOR基質蛋白と結合するOral presentation
- Conference on Patho-Physiological aspects of BCAA, Mar. 2003, English, Takanawa Prince Hotel, Tokyo, Japan, International conferenceCrosstalk between energy sensing system and mTOR signaling pathway[Invited]Invited oral presentation
- Conference on Patho-Physiological aspects of BCAA, Mar. 2003, English, Takanawa Prince Hotel, Tokyo, Japan, International conferenceIdentification and Characterization of Raptor, a novel binding partner of mTOR[Invited]Invited oral presentation
- 第1回ヒトプロテオーム学会, Feb. 2003, Japanese, 産業技術総合研究所共用講堂(つくば市), Japan, Domestic conferenceヒトプロテオミクス研究のためのESTコンセンサス配列データベースの有効利用Oral presentation
- 大阪大学蛋白質研究所セミナー、プロテオーム・ペプチドーム最前線 ー解析法の実際と応用ー, Feb. 2003, Japanese, 大阪大学蛋白質研究所, 大阪大学蛋白質研究所, Japan, Domestic conference質量分析法とコンセンサス配列データベースを利用する新規蛋白質の探索[Invited]Nominated symposium
- 第25回日本分子生物学会年会, Dec. 2002, Japanese, 日本分子生物学会, パシフィコ横浜, Japan, Domestic conferenceミトコンドリアリボソームの比較解析:構成と機能の進化Poster presentation
- 第25回日本分子生物学会年会, Dec. 2002, Japanese, 日本分子生物学会, パシフィコ横浜, Japan, Domestic conference新規mTOR結合蛋白質p150RaptorのmTOR-4EBP1 Signalingにおける機能の解析Poster presentation
- 第25回日本分子生物学会年会, Dec. 2002, Japanese, 日本分子生物学会, パシフィコ横浜, Japan, Domestic conference新規mTOR結合蛋白質p150RaptorのmTOR-p70S6K Signalingにおける機能の解析Poster presentation
- 第25回日本分子生物学会年会, Dec. 2002, Japanese, 日本分子生物学会, パシフィコ横浜, Japan, Domestic conferenceアミノ酸バランスを感知して細胞成長を制御するmTOR Signaling[Invited]Nominated symposium
- 第25回日本分子生物学会年会, Dec. 2002, Japanese, 日本分子生物学会, パシフィコ横浜, Japan, Domestic conference新規mTOR結合蛋白質p150Raptorの精製と質量分析法による同定・構造解析Poster presentation
- 第14回分子糖尿病シンポジウム, Dec. 2002, Japanese, ホテルオオサカサンパレス, JapanmTOR-scaffold蛋白p150-Raptorのクローニングとインスリン作用における役割Oral presentation
- Infocomプロテオミクスセミナー(大阪会場), Nov. 2002, Japanese, インフォコム株式会社, 梅田スカイビル, Japan, Domestic conferenceプロテオミクスにおけるコンセンサス配列データベースの有効利用[Invited]Public discourse
- 日本生物物理学会第40回年会, Nov. 2002, Japanese, 日本生物物理学会, 名古屋大学東山地区(名古屋市千種区不老町), Japan, Domestic conferenceウシ視細胞ラフト様膜分画に局在する脂質と蛋白質 : 脊椎動物視細胞のraftとsignalplexOral presentation
- FEBS 2002 Meeting, Oct. 2002, English, Istambul, Turkey, International conferenceActivity of Xenopus Src kinase in the course of maturation, fertilization and early embryonic cell cycles
- CBI学会第222回研究講演会「創薬と質量分析の進歩」, Oct. 2002, Japanese, 情報計算化学生物学会(CBI学会), 日本化学会化学会館, Japan, Domestic conferenceプロテオミクスと質量分析 ~核酸配列データベースを用いた未知蛋白質の探索~[Invited]Nominated symposium
- 第75回日本生化学会大会, Oct. 2002, Japanese, 日本生化学会, 国立京都国際会館, Japan, Domestic conference質量分析法とヒト暫定共通配列データベースを用いた新規mTOR結合蛋白質p150TSWの同定と構造解析[Invited]Nominated symposium
- 第75回日本生化学会大会(京都), Oct. 2002, Japanese, 日本生化学会, 国立京都国際会館, Japan, Domestic conference新規mTOR結合蛋白質p150TSWの精製とその機能解析Poster presentation
- 第75回日本生化学会大会(京都), Oct. 2002, Japanese, 日本生化学会, 国立京都国際会館, Japan, Domestic conferencemTORシグナル伝達経路とAMP-activated kinaseの相互作用の解析Poster presentation
- 文部科学省科学研究費特定領域研究「ゲノム」4領域、2002年度合同班会議, Aug. 2002, Japanese, 神戸ポートピアホテル, Japan, Domestic conference哺乳細胞において細胞成長を司るシグナル伝達分子群のプロテオーム解析と機能同定
- 第29回BMSコンファレンス, Jul. 2002, Japanese, 日本質量分析学会, 八ヶ岳ロイヤルホテル, Japan, Domestic conferenceBiosignal Mass Spectrometry[Invited]Public symposium
- Gordon Research Conference, Second Messengers & Protein Phosphorylation, Jun. 2002, English, Kimball Union Academy, Meriden, NH, United States, International conferenceCrosstalk between mTOR and AMP-activated protein kinase
- Gordon Research Conference, Second Messengers and Protein Phosphorylation, Jun. 2002, English, Kimball Union Academy, Meriden, NH, United States, International conference, Co-authored internationallyIdentification of p150TSW, a Target of Rapamycin (TOR)-Scaffold Protein containing WD-repeats
- 50th ASMS Conference on Mass Spectrometry and Allied Topics, Jun. 2002, English, American Society for Mass Spectrometry, Orlando, Florida, United StatesThe Complete Amino Acid Sequence Determination of a Novel Protein by Mass Spectrometry with the Tentative Human Consensus Sequence DatabasePoster presentation
- 第45回日本糖尿病学会年次学術集会, May 2002, Japanese, 東京国際フォーラム(東京都千代田区丸の内三丁目5番1号), Japan, Domestic conference新規mTOR結合蛋白(p150TORAP)の同定とインスリン作用における役割Poster presentation
- 第50回質量分析総合討論会, May 2002, Japanese, 日本質量分析学会, 京都工芸繊維大学松ヶ崎キャンパス, Domestic conferenceNano-ESI-Q-TOF-MSを用いた相同性の高い複数の蛋白質からなる混合物の解析Poster presentation
- 第50回質量分析総合討論会, May 2002, Japanese, 日本質量分析学会, 京都工芸繊維大学松ヶ崎キャンパス, Japan, Domestic conferenceNano-ESI-Q-TOF-MSを用いたmammalian target of rapamycin (mTOR)のin vivoリン酸化部位の同定と解析Oral presentation
- 第50回質量分析総合討論会, May 2002, Japanese, 日本質量分析学会, 京都工芸繊維大学松ヶ崎キャンパス, Japan, Domestic conferenceUsefulness of the Tentative Human Consensus Sequence Database in Protein Identification by Mass SpectrometryOral presentation
- 第24回日本分子生物学会年会(横浜), Dec. 2001プロテオミクス的手法によるゼノパス卵受精成立の場の解析
- 第24回日本分子生物学会年会(横浜), Dec. 2001ゼノパス卵SrcファミリーチロシンキナーゼXykの構造解析と発現
- 第24回日本分子生物学会年会(横浜), Dec. 2001AMP-activated protein kinaseによるp70 S6 kinase活性制御機構の解析
- 第24回日本分子生物学会年会(横浜), Dec. 2001質量分析法によるmTORリン酸化部位の解析
- 第24回日本分子生物学会年会(横浜), Dec. 2001酵母の出芽部位に局在するElm1タンパク質の機能解析
- 第24回日本分子生物学会年会(横浜), Dec. 2001出芽酵母のミトコンドリアリボソーム蛋白質遺伝子の同定と解析
- 第24回日本分子生物学会年会、ワークショップ(横浜), Dec. 2001ラパマイシン標的蛋白質mTORを介したシグナル伝達系の研究
- 質量分析講習会アドバンストコース「MSによるプロテオーム研究立ち上げに何が必要か」, Nov. 2001, Japanese, 日本質量分析学会, Domestic conference新しいMSのパワーを知る、プロテオーム関連MS、Q-TOF-MS[Invited]Public discourse
- 第74回日本生化学会大会(京都), Oct. 2001, Japanese, 日本生化学会, 国立京都国際会館, Japan, Domestic conference蛋白合成系と蛋白質分解系を制御する分子TORを介した情報伝達機構[Invited]Nominated symposium
- 第74回日本生化学会大会(京都), Oct. 2001, Japanese, 日本生化学会, 国立京都国際会館ロイシン誘導体Ac-Leu-NH2を用いたアミノ酸-mTORシグナル伝達機構の解析Poster presentation
- 文部科学省科学研究費特定領域研究C「ゲノム」4領域、2001年度合同班会議, Aug. 2001, Japanese, 神戸ポートピアホテル哺乳動物におけるシグナル伝達機構解明のためのプロテオーム解析の基盤研究
- 酵母遺伝学フォーラム第34回研究報告会(京都), Jul. 2001酵母の出芽部位に局在するElm1タンパク質の機能解析
- 第54回日本細胞生物学会大会(岐阜), May 2001, Japaneseアミノ酸によるp70S6キナーゼの活性化に対するmTORとPDK1依存性シグナルの役割
- 第54回日本細胞生物学会大会(岐阜), May 2001, Japanese質量分析法によって見出されたmTORリン酸化部位の解析
- 第54回日本細胞生物学会大会(岐阜), May 2001, JapanesemTORを介した情報伝達系の研究
- 第3回ワークショップ「微生物ゲノム研究のフロンティア」, Feb. 2001, Japanese, 文部省科学研究費補助金・特定領域研究『統合ゲノム』, かずさアカデミアホール(千葉県木更津市), Japan, Domestic conferenceウェルシュ菌のプロテオーム解析Poster presentation
- 第23回日本分子生物学会年会(神戸), Dec. 2000, Japanese, 日本分子生物学会, 神戸国際展示場, Domestic conferenceProteomics analysis of Clostridium perfringens extracelluar proteinPoster presentation
- 第23回日本分子生物学会年会(神戸), Dec. 2000, Japanese, 日本分子生物学会, 神戸国際展示場, Domestic conferenceProteomics analysis of VirR/VirS regulated-protein in Clostridium perfringensPoster presentation
- 第23回日本分子生物学会年会(神戸), Dec. 2000, Japanese, 日本分子生物学会, 神戸国際展示場, Japan, Domestic conferenceLeucine誘導体L-Leu8MAPによるmTOR情報伝達系の活性化Poster presentation
- 第73回日本生化学会大会(横浜), Oct. 2000, Japanese, 日本生化学会, パシフィコ横浜, Japan, Domestic conferenceラパマイシン標的蛋白質mTORとPhosphoinositide dependent kinaseによるp70 S6 kinaseの活性化機構の解析Poster presentation
- 第43回日本糖尿病学会年次学術集会(名古屋), May 2000ラパマイシン標的蛋白質mTORキナーゼとPhospho-inositide dependent kinase (PDK1)によるp70 S6キナーゼ(p70)の活性化機構の解析
- 第3回腸管出血性大腸菌感染症シンポジウム(東京), Jul. 1998Site-directed mutagenesisを用いた抗Stx2マウスモノクローナル抗体のエピトープの解析
- 第71回日本細菌学会総会(松本), Apr. 1998, Japanese, 日本細菌学会, 長野県松本文化会館、松本市総合体育館, Japan, Domestic conferenceヒトや種々の動物の血清中に検出される抗VT1及び抗VT2中和抗体の意義Poster presentation
- 第72回日本感染症学会(大阪), Apr. 19981997年、当研究部での腸管出血性大腸菌O157患者の検出状況
- 第78回日本細菌学会関東支部総会, Oct. 1997, Japanese, 横浜ロイヤルパークホテルニッコー, Japan, Domestic conferenceVT2に対するマウスモノクローナル抗体のエピトープ解析Oral presentation
- 第70回日本生化学会大会, Sep. 1997, Japanese膜結合型グアニル酸シクラーゼのリン酸化部位
- 第2回腸管出血性大腸菌感染症シンポジウム(堺), Aug. 19971996年全国アンケートによる大腸菌感染症O157の実態調査
- 第77回日本細菌学会関東支部総会, Jun. 1997, Japanese, アルカディア市ヶ谷, Domestic conference腸管出血性大腸菌O157の産生するベロ毒素に対する吸着剤のin vitro薬効評価Nominated symposium
- 第77回日本細菌学会関東支部総会, Jun. 1997, Japanese, アルカディア市ヶ谷, Japan, Domestic conference腸管出血性大腸菌O157:H7の非培養検査法の評価Poster presentation
- 3rd International Symposium and Workshop on Shiga Toxin (Verocytotoxin)-Producing Escherrichia coli Infection (VTEC '97), Jun. 1997, English, Renaissane Harborplace Hotel, Baltimore, Maryland, United States, International conferenceQuestionnaire-based Clinical Aspects of VTEC Infection in Japan, 1996Poster presentation
- 3rd International Symposium and Workshop on Siga Toxin (Verocytotoxin)-Producing Escherichia coli Infections (VTEC '97), Jun. 1997, English, Renaissane Harborplace Hotel, Baltimore, Maryland, United States, International conferenceEarly use of antibiotics for STEC O157 infection rduces the risk of hemolytic uremic syndromeInvited oral presentation
- 3rd International Symposium and Workshop on Shiga Toxin (Verocytotoxin)-Producing Escherrichia coli Infection (VTEC '97), Jun. 1997, English, Renaissane Harborplace Hotel, Baltimore, Maryland, United States, International conferenceFailure of immune response to Shiga toxin-producing Escherichia coli O157 lipopolysaccharide antigen in healthy carriersPoster presentation
- 3rd International Symposium and Workshop on Shiga Toxin (Verocytotoxin)-Producing Escherrichia coli Infection (VTEC '97), Jun. 1997, English, Renaissane Harborplace Hotel, Baltimore, Maryland, United States, International conferenceRapid Disappearance of Fecal Verotoxins in Patients with VTEC O157:H7 Infection who were Given Antibiotics at Early Stage of the DiseasePoster presentation
- 3rd International Symposium and Workshop on Shiga Toxin (Verocytotoxin)-Producing Escherrichia coli Infection (VTEC '97), Jun. 1997, English, Renaissane Harborplace Hotel, Baltimore, Maryland, United States, International conferenceTwo Major Clones were Found during a Crisis of VTEC O 157:H7 (VT1+, VT2+) Infection in Japan, 1996Poster presentation
- The 6th China-Japan International Congress of Microbiology, Jun. 1997, EnglishHemolytic Urine Syndrome[Invited]Nominated symposium
- 第32回日本小児腎臓病学会学術集会(大阪), Jun. 1997ベロ毒素産生性大腸菌O121: H19による溶血性尿毒症症候群の1幼児例
- 第32回日本小児腎臓病学会学術集会(大阪), Jun. 1997病原性大腸菌O165によると考えられた溶血性尿毒症症候群の2例
- 第71回日本感染症学会総会, Apr. 1997, Japanese, ロイトン札幌(札幌市中央区北1条西11丁目), Japan, Domestic conference腸管出血性大腸O157の迅速検出キットの評価Oral presentation
- 第70回日本細菌学会総会(宇都宮), Mar. 1997, Japanese, 日本細菌学会, 栃木県総合文化センター, Japan, Domestic conference1996年日本各地で分離された腸管出血性大腸菌O157の分子疫学Nominated symposium
- 第70回日本細菌学会総会(宇都宮), Mar. 1997, Japanese, 日本細菌学会, 栃木県総合文化センター, Japan, Domestic conferenceヒト血清中のベロ毒素2(VT2)中和因子Nominated symposium
- 第70回日本細菌学会総会(宇都宮), Mar. 1997, Japanese, 日本細菌学会, 栃木県総合文化センター, Japan, Domestic conference腸管出血性大腸菌O157に対する乳酸菌、ビフィズス菌の感染予防効果Nominated symposium
- 第70回日本細菌学会総会(宇都宮), Mar. 1997, Japanese, 日本細菌学会, 栃木県総合文化センター, Domestic conference一般健康成人からの大腸菌O157の分離頻度Nominated symposium
- 第70回日本細菌学会総会(宇都宮), Mar. 1997, Japanese, 日本細菌学会, 栃木県総合文化センター, Japan, Domestic conferenceベロ毒素産生性大腸菌O157LPSに対する血中抗体価にみられる小児と成人との差異Nominated symposium
- The 32nd Joint Conference of Cholera and Related Diarrheal Diseases Panel in U.S.-Japan Cooperative Medical Science Program, Nov. 1996, English, Nagasaki University Pompe Hall, Japan, International conferenceHemolytic uremic syndrome associated with verotoxin-producing Escherichia coliOral presentation
- The 32nd Joint Conference of Cholera and Related Diarrheal Diseases Panel in U.S.-Japan Cooperative Medical Science Program, Nov. 1996, English, Nagasaki University Pompe Hall, Japan, International conferenceIdentification of the functional regions of the superantigen Yersinia pseudotuberculosis-derived mitogen (YPM) by characterizing a novel variant molecule and by using the synthetic peptide fragmentsOral presentation
- 第76回日本細菌学会関東支部総会, Nov. 1996, English, 東京女子医科大学弥生記念講堂(東京都新宿区河田町8-1), Japan, Domestic conference本年国内で集中発生したVTEC O157 のパルスフィールドゲル電気泳動法による分子疫学Oral presentation
- 第76回日本細菌学会関東支部総会, Nov. 1996, Japanese, 東京女子医科大学弥生記念講堂(東京都新宿区河田町8-1), Japan, Domestic conference本年当院で分離したVTEC O157と岡山・邑久町での集団発生株との類似性Oral presentation
- 第76回日本細菌学会関東支部総会, Nov. 1996, Japanese, 東京女子医科大学弥生記念講堂(東京都新宿区河田町8-1), Japan, Domestic conferenceVTEC O157感染症に対するグロブリン製剤の有用性Oral presentation
- 第76回日本細菌学会関東支部総会, Nov. 1996, Japanese, 東京女子医科大学弥生記念講堂(東京都新宿区河田町8-1), Japan, Domestic conference本年集中発生したHUSのVTEC O157 LPSに対する血中抗体の検出頻度Oral presentation
- 第76回日本細菌学会関東支部総会, Nov. 1996, Japanese, 東京女子医科大学弥生記念講堂(東京都新宿区河田町8-1), Japan, Domestic conference便の増菌培養液を用いたPCRによるVTEC感染症の迅速診断Oral presentation
- 第28回日本小児感染症学会, Nov. 1996, Japanese, 日本小児感染症学会, 砂防会館(東京都千代田区平河町2-7-5), Japan, Domestic conferenceO157大腸菌による集団食中毒から2次感染した一例Oral presentation
- 第28回日本小児感染症学会, Nov. 1996, Japanese, 日本小児感染症学会, 砂防会館(東京都千代田区平河町2-7-5), Japan, International conference当院でのベロ毒素産生性大腸菌O157によるHUSの散発例-患者の姉から原因菌が検出された意義-Oral presentation
- 第28回日本小児感染症学会, Nov. 1996, Japanese, 日本小児感染症学会, 砂防会館(東京都千代田区平河町2-7-5), Japan, Domestic conferenceパルスフィールドゲル電気泳動法によるベロ毒素産生性大腸菌(VTEC) O157の分子疫学Oral presentation
- 第28回小児感染症学会, Nov. 1996, Japanese, 日本小児感染症学会, 砂防会館(東京都千代田区平河町2-7-5), Domestic conferenceベロ毒素産生性大腸菌(VTEC) O157検出のためのPCR法の有用性Oral presentation
- The International Congress for Tripical Medicine and Malaria, Nov. 1996, English, Nagasaki University, Domestic conferenceIncidence of Novel Subtype Heat-Stable Enterotoxin Genes Among Non-Epidemic Yersinia enterocolitica Strains
- 第43回毒素シンポジウム, Jul. 1996, Japanese, 加賀観光ホテル(加賀市), Japan, Domestic conferenceスーパー抗原YPMのリンパ球増殖活性を特異的に阻害するペプチドPoster presentation
- 第43回毒素シンポジウム, Jul. 1996, Japanese, 加賀観光ホテル(加賀市), Japan, Domestic conferenceスーパー抗原YPMのサブタイプ分子YPMbの精製、構造決定およびその性質Oral presentation
- 日本小児腎臓病学会第31回学術集会, Jul. 1996, Japanese, 前橋商工会議所会館, Domestic conference腸管出血性大腸菌O157によるHUSの集中発生とその分子疫学Oral presentation
- 44th ASMS Conference on Mass Spectrometry and Allied Topics, May 1996, English, American Society for Mass Spectrometry, Oregon Convetion Center, Portland, United States, International conferenceMALDI-TOF MS of Oligosaccharides Derivatized with 4-Aminobenzoic Acid 2-(Dimethylamino)ethyl Ester
- 第69回日本細菌学会総会(福岡), Mar. 1996, English, 日本細菌学会, アクロス福岡, Japan, Domestic conferenceYersinia enterocolitica産生するY-STbの遺伝子塩基配列および血清型O:5 Biotype 1Aとの高い相関Poster presentation
- 第69回日本細菌学会総会(福岡), Mar. 1996, Japanese, 日本細菌学会, アクロス福岡, Domestic conferenceスーパー抗原YPMのサブタイプ分子YPMbの遺伝子クローニングと大腸菌での発現Poster presentation
- 第69回日本細菌学会総会(福岡), Mar. 1996, Japanese, 日本細菌学会, アクロス福岡, Japan, Domestic conferenceエルシニア菌の産生するスーパー抗原(YPM)の大量調製法の確立Poster presentation
- 第69回日本細菌学会総会(福岡), Mar. 1996, Japanese, 日本細菌学会, アクロス福岡, Japan, Domestic conferenceスーパー抗原YPMのサブタイプ分子YPMbの精製とその性状Poster presentation
- 第69回日本細菌学会総会(福岡), Mar. 1996, Japanese, 日本細菌学会, アクロス福岡, Japan, Domestic conferenceスーパー抗原YPMのマイトジェン活性を阻害するYPM部分ペプチドの調製Poster presentation
- The 31st Joint Conference of Cholera and Related Diarrheal Diseases, Dec. 1995, English, The Unitted States-Japan Cooperative Medical Science Program, Kiawah Island, SC, USA, United States, International conference, Co-authored internationallyPurification and characterization of a novel superantigen produced by Yersinia pseudotuberculosisOral presentation
- 第74回日本細菌学会関東支部総会, Oct. 1995, English, 駒場エミナース(東京都目黒区大橋2-19-5), Japan, Domestic conference, Co-authored internationallyMolecular epidemiology of Yersinia pseudotuberculosis by pulsed-field gel electrophoresisOral presentation
- 第74回日本細菌学会関東支部総会, Oct. 1995, Japanese, 駒場エミナース(東京都目黒区大橋2-19-5), Japan, Domestic conference耐熱性エンテロトキシン毒性ドメインのN末端側近傍に存在するアミノ酸残基の毒性に及ぼす役割Oral presentation
- 第42回毒素シンポジウム, Aug. 1995, Japanese, 石橋文化センター(久留米市野中町1015), Japan, Domestic conference成熟毒素分子として“プロ領域”を含む耐熱性エンテロトキシンY-STcの前駆体蛋白質とリコンビナントY-STcの構造Poster presentation
- 第42回毒素シンポジウム, Aug. 1995, Japanese, 石橋文化センター(久留米市野中町1015), Japan, Domestic conference新規スーパー抗原Yersinia pseudotuberculosis-derived Mitogen (YPM)をコードする遺伝子の塩基配列およびその遺伝子頻度における地理的相違Oral presentation
- The 9th International Congress of Immunology, Jul. 1995, English, International conferenceSequence Analysis of the Gene for a Novel Superantigen Produced by Yersinia pseudotuberculosis and Characterization of the Recombinat Protein
- 5th International Kawasaki Disease Symposium (Fukuoka), May 1995, English, ACROS Fukuoka, International Convention Hall, Japan, International conferenceEstablishment of a novel superantigen produced by Yersinia pseudotuberculosis and its association with systemic Kawasaki disease-like symptoms
- Annual Meeting of Professional Research Scientists, Experimental Biology 95 (Atlanta, GA, USA), Apr. 1995, EnglishGenetic analysis of a novel superantigen produced by Yersinia pseudotuberculosis and its effect in acute phase patients
- 第68回日本細菌学会総会(京都府相楽郡), Mar. 1995, Japanese, 日本細菌学会, けいはんな学研都市・けいはんなプラザ, Japan, Domestic conferenceST毒素ファミリーのうち最大分子量を有するYersinia enterocolitica,/i>の新規なY-STサブタイプの遺伝子クローニングと大腸菌での発現Poster presentation
- 第68回日本細菌学会総会(京都府相楽郡), Mar. 1995, English, 日本細菌学会, けいはんな学研都市・けいはんなプラザ, Japan, Domestic conferenceYersinia enterocoliticaの2種の新規なST毒素遺伝子の特異プローブの調製とその分布Poster presentation
- 第68回日本細菌学会総会(京都府相楽郡), Mar. 1995, Japanese, 日本細菌学会, けいはんな学研都市・けいはんなプラザ, Japan, Domestic conferenceYersinia pseudotuberculosis由来新規スーパー抗原をコードする遺伝子の分布Poster presentation
- 第68回日本細菌学会総会(京都府相楽郡), Mar. 1995, Japanese, 日本細菌学会, けいはんな学研都市・けいはんなプラザ, Japan, Domestic conferenceYersinia pseudotuberculosisの産生するスーパー抗原の遺伝子解析と組換体蛋白の発現Poster presentation
- The 30th Joint Conference of Cholera and Related Diarrheal Diseases Panel, Dec. 1994, English, Cholera and Related Diarrheal Diseases Panel, The Unitted States-Japan Cooperative Medical Science Program, Kyushu University Alumnus Hall, Japan, International conferenceAmino acid sequences of newly recognized two subtypes of heat-stable enterotoxin produced by Yersinia enterocoliticaOral presentation
- 第24回日本免疫学会総会・学術集会, Nov. 1994, Japanese, 日本免疫学会, 国立京都国際会館, Japan, Domestic conferenceYersinia pseudotuberculosisの産生するスーパー抗原の高度精製とその遺伝子のクローニング
- 第14回川崎病研究会(和歌山), Oct. 1994, Japanese, 和歌山市民会館, Japan, Domestic conferenceYersinia pseudotuberculosisの産生するスーパー抗原の高度精製とその遺伝子解析
- 大阪大学蛋白質研究所セミナー 蛋白質の一次構造解析法の現状と展望, Oct. 1994, Japanese, 大阪大学蛋白質研究所, 大阪大学蛋白質研究所, Japan, International conference質量分析法による糖蛋白質の糖鎖構造解析[Invited]Public discourse
- 日本動物学会第65回大会(名古屋), Oct. 1994精子活性化ペプチド受容体の構造
- 6th International Symposium on Yersinia (Rome, ITALY), Sep. 1994, EnglishPurification and cloning of a gene encoding a novel superantigen produced by a clinical strain of Yersinia pseudotuberculosis
- 平成6年度日本動物学会北海道支部大会(旭川), Aug. 1994, Japaneseバフンウニ精子活性化ペプチド受容体の構造
- 第41回毒素シンポジウム, Jul. 1994, Japanese, アルカディア市ヶ谷 私学会館(東京都千代田区九段北4-2-25), Japan, Domestic conferenceYersinia pseudotuberculosis由来スーパー抗原の高比活性精製標品の分離とその蛋白質化学的性質Oral presentation
- The 42nd ASMS Conference on Mass Spectrometry and Allied Topics, Jun. 1994, English, American Society for Mass Spectrometry, The Hyatt Regency Hotel Chicago, IL, United States, International conferenceChemical Derivatization for High-Sensitive Detection of Oligosaccharides in Electrospray Ionization Mass SpectrometryPoster presentation
- 第67回日本細菌学会総会, Mar. 1994, Japanese, 日本都市センター(東京都新宿区河田町2-4-1), Japan, Domestic conferenceYersinia pseudotuberculosisの産生するスーパー抗原精製法の検討Poster presentation
- 第66回日本生化学会大会(東京), Oct. 1993, Japanese, 日本生化学会, 東京大学教養学部, Japan, Domestic conference大腸菌内で合成した植物フェレドキシン分子の不均一性Poster presentation
- 第66回日本生化学会大会(東京), Oct. 1993, Japanese, 日本生化学会, 東京大学教養学部, Japan, Domestic conferenceエレクトロスプレーイオン化質量分析法による糖蛋白質糖鎖のミクロヘテロジェネイティの解析Poster presentation
- 第66回日本生化学会大会(東京), Oct. 1993, Japanese, 日本生化学会, 東京大学教養学部, Japan, Domestic conferenceエレクトロスプレーイオン化質量分析法によるオリゴ糖高感度分析:2-Diethylaminoethyl 4-aminobenzoate誘導体化Oral presentation
- 第40回毒素シンポジウム, Jul. 1993, Japanese, 花びしホテル(函館市湯川町1-16-18), Domestic conferenceYersinia pseudotuberculosisの産生するスーパー抗原の精製と性状Oral presentation
- 第40回毒素シンポジウム, Jul. 1993, Japanese, 花びしホテル(函館市湯川町1-16-18), Japan, Domestic conferenceYersinia enterocolitica 84-50株および86-11株の産生する2種類の新しい耐熱性エンテロトキシンの単離、構造決定Oral presentation
- 第66回日本細菌学会総会, Mar. 1993, Japanese, 名古屋国際会議場(名古屋市熱田区熱田西町1番1号), Japan, Domestic conferenceYersinia enterocoliticaの産生する新しい耐熱性エンテロトキシンの性状と一次構造Poster presentation
- 第66回日本細菌学会総会, Mar. 1993, Japanese, 名古屋国際会議場(名古屋市熱田区熱田西町1番1号), Japan, Domestic conference, Co-authored internationallyVibrio cholerae O1の産生する耐熱性エンテロトキシンの一次構造Poster presentation
- 第29回ペプチド化学討論会, Nov. 1991, Japanese, 日本ペプチド学会, 共立講堂(東京都千代田区神田一ツ橋2-2-1 共立女子大学), Japan, Domestic conference新しく単離されたシスチン含有精子活性化ペプチドのタンデム質量分析法による一次構造解析Poster presentation
- 日本動物学会第62回大会(岡山), Oct. 1991, Japanese, 日本動物学会, 岡山大学教養部, Japan, Domestic conferenceIdentification and characterization of specific receptors for sperm-activating peptide III (SAP-III)Oral presentation
- 1st Biennial International Conference on Amino Acid Research, Aug. 1991, English, Kyoto International Conference Hall, Japan, International conferenceThe presence of o-, m-, and p-bromophenylalanines and bromohistidine in sperm-activating peptidesPoster presentation
- 第24回若手ペプチド夏の勉強会(東浦町・淡路島), Aug. 1991, Japanese, 東浦サンパーク(津名郡東浦町、淡路島), Japan, Domestic conference受精における精子活性化機構:卵ジェリーに含まれる精子活性化ペプチドとα-アミノイソ酪酸 (Aib) の効果Oral presentation
- The 28th Symposium on Peptide Chemistry, Oct. 1990, Japanese, 日本ペプチド学会, 千里協栄生命ホール(大阪府豊中市千里西1-1-10), Japan, Domestic conferencePrimary Structures of Bromophenylalanine-containing Sperm-Activating PeptidesOral presentation
- 日本動物学会第61回大会, Oct. 1990, Japanese, 日本動物学会, 新潟大学工学部, Domestic conferenceIdentification of a novel amino acid, L-ortho-bromopehylalanine, in sperm-activating peptides from the egg jelly of the sea urchin Tripneustes gratillaOral presentation
- 7th International Echinoderm Conference, Sep. 1990, English, Hotel Chateutel Akanezaki, Atami, Japan, International conferenceTwo novel brominated amino acids-containig sperm activating peptides isolated from the egg jelly of sea urchins, Tripneustes gratilla and Clypeaster japonicusPoster presentation
- 第22回若手ペプチド夏の勉強会(高遠町・長野県), Jul. 1989, Japanese, Japan, Domestic conference精子活性化ペプチドⅠ(SAP-I)の構造活性相関Oral presentation
- 59th Annual Meetings of the Zoological Society of Japan, Oct. 1988, Japanese, the Zoological Society of Japan, 札幌医科大学, Domestic conferenceVariations in the structures of sperm activating peptides from the egg jelly of sea urchins in order EchinoidaOral presentation
- 第21回若手ペプチド夏の勉強会(阿南市・徳島県), Aug. 1988, Japanese, JapanSperm Activating Peptide (SAP) の単離・精製・構造決定およびその生理作用Oral presentation
- The 58th Annual Meetings of the Zoological Society of Japan, Oct. 1987, Japanese, 日本動物学会, 富山大学, Japan, Domestic conferenceSpecificity of Sperm Activating PeptidesOral presentation
- The 58th Annual Meeting of the Zoological Society of Japan, Oct. 1987, Japanese, the Zoological Society of Japan, 富山大学, Japan, Domestic conferencePurification and Structure of Sperm-Activating Peptides from the Egg Jelly of the Sea Urchin Diadema setosumOral presentation
- 6th International Echinoderm Conference (Victoria, CANADA), Aug. 1987, EnglishTaxonomical significance of respiratory stimulation of sea urchin spermatozoa by egg associated substancesOral presentation
- 昭和61年度日本動物学会中部支部秋季例会, Nov. 1986, Japanese, 日本動物学会中部支部, 富山市, Japan, Domestic conferenceSperact結合量の測定、および結合部位の局在性Oral presentation
- 昭和61年度日本動物学会中部支部秋季例会, Nov. 1986, Japanese, 日本動物学会中部支部, 富山市, Domestic conferenceAlloresact(アロレスアクト)誘導体の分離、精製および構造Oral presentation
- 日本動物学会第57回大会, Oct. 1986, Japanese, 日本動物学会, 九州大学箱崎法文系キャンパス, Japan, Domestic conferenceThe effect of speract on the mobility of a high molecular weight protein of the sea urchin spermatozoa on SDS-polyacrylamide gelsOral presentation
- 日本動物学会第57回大会, Oct. 1986, Japanese, 日本動物学会, Fukuoka, Japan, Domestic conferenceIsolation of sperm activating peptides from egg jelly of the sea urchin, Glyptocidaris crenularisOral presentation
- The 5th International Symposium on Spermatology, Aug. 1986, English, Fujiyoshida City, YAMANASHI, Japan, International conference, Co-authored internationallySperm-activating peptides from the egg jelly of various species of sea urchin.Oral presentation
- 昭和61年度日本動物学会中部支部春季例会(津), May 1986, Japaneseホンウニ類卵ジェリー中の精子呼吸促進ペプチドOral presentation
■ Research Themes- 日本学術振興会, 科学研究費助成事業, 基盤研究(C), 神戸大学, Apr. 2023 - Mar. 2026, Coinvestigator筋細胞に生じる高齢者特有のプロテオスタシスの低下を軽減する分子機序の解明
- 日本学術振興会, 科学研究費助成事業 基盤研究(C), 基盤研究(C), 神戸大学, Apr. 2022 - Mar. 2025, Coinvestigator熱帯熱マラリア原虫生殖母体期の感染赤血球における細胞接着機構の解析
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, Apr. 2020 - Mar. 2023, CoinvestigatorPL標識法による筋線維芽細胞の力伝達に関わる新機能探索と筋力低下予防への応用
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, Apr. 2017 - Mar. 2020, CoinvestigatorAnalysis of differential S-palmitoylation of the human and rodent beta3 adrenergic receptorTo clarify the functions and effects of beta-3 adrenergic receptor (β3AR) on obesity, type II diabetes and overactive bladder, we focused on S-palmitoylation, a post-translational modification of β3AR. Interestingly, number and sites of palmitoylation modifications of human and mouse β3AR are distinct, and the mechanism of the increase in receptor expression on the plasma membrane by a β3AR specific agonist, mirabegron, is also distinct. Multiple S-palmitoylation of different sites differentially regulates the human β3AR, and differential S-palmitoylation distinguishes human and rodent β3ARs, potentially contributing to species-specific differences in the clinical efficacy of β3AR-directed pharmacological approaches to disease. In addition, we have generated and analyzed humanized β3AR knock-in mice to clarify the pathophysiological relevances of differential S-palmitoylation on β3AR.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (A), Grant-in-Aid for Scientific Research (A), Kobe University, 01 Apr. 2012 - 31 Mar. 2015This research project was aimed to understand the molecular bases, which enable the global genomic nucleotide excision repair (GG-NER) pathway to efficiently survey genomic DNA for damage caused by various environmental stresses. By using the defined cell-free GG-NER system reconstituted with purified recombinant protein factors, it was shown that certain endogenous DNA lesions, such as abasic sites, facilitate the damage recognition process in GG-NER, and that DNA repair efficiency is affected by the topological state of damaged DNA as well as protein phosphorylation. We also elucidated novel roles of ubiquitination and SUMOylation of the xeroderma pigmentosum group C (XPC) protein in recognition of ultraviolet (UV)-induced DNA photolesions mediated by the UV-damaged DNA binding protein complex. Finally, single molecule imaging experiments revealed one-dimensional diffusion of the XPC protein during the search for lesions along DNA.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (B), Grant-in-Aid for Scientific Research (B), Kobe University, 2009 - 2011The complete genome sequences of four Helicobacter pylori strains isolated from Japan were determined. A phylogenetic tree of concatenated well-defined core genes supported divergence of the East Asian lineage from the European lineage ancestor, and then from the Amerind lineage ancestor. Phylogenetic profiling revealed a large difference in the repertoire of outer membrane proteins. The results define H. pylori East Asian lineages and provide essential information for understanding their pathogenesis. We investigated metabolome analysis using liquid chromatography-mass spectrometry, gas chromatography-mass spectrometry. Lactic acid was upregulated in H. pylori infected AGS(gastric cancer cell line) cells and serum of gastric cancer patients. In contrast, malic acid was downregulated in H. pylori infected AGS cells and serum of gastric cancer patients.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Exploratory Research, Grant-in-Aid for Exploratory Research, Kobe University, Apr. 2005 - Mar. 2007, Principal investigatorアミノ酸バランスを感知するシグナル伝達機構と核酸生合成の研究再狭窄抑制剤、T細胞増殖抑制剤、抗癌剤としての薬効が注目されている薬剤ラパマイシンの哺乳動物細胞内の標的タンパク質がmammalian Target of Rapamycin (mTOR)である。mTORはアミノ酸濃度などの細胞が活発に増殖できる環境条件を感知し細胞増殖、細胞成長制御システムを司る情報伝達系の中枢分子である。 細胞増殖にはDNA複製が不可欠であり、そのためには原料となるプリンヌクレオチド、ピリミジンヌクレオチドが大量に必要となる。これらの核酸生合成はグルタミンやアスパラギン酸グリシンなどのアミノ酸を原料とし、核酸の新生にはアミノ酸が不可欠である。細胞の分裂に必要なDNAを複製するためには原料となる大量のアミノ酸を必要とすることから、我々はmTORを中枢としたアミノ酸感知-細胞成長制御系と核酸生合成系とが深く関わっているのではないかと考え、これを裏付ける分子の探索を行った。 mTOR複合体を構成するraptorおよびmLST8と相互作用する分子の中で核酸生合成に関与する分子を探索したところ、ピリミジン生合成経路において重要な役割を担っているcarbamoyl phosphate synthetase, aspartate transcarbamoylase, dihydroorotase (CAD)が見出された。 この分子はraptorおよびmLST8のWDドメインと相互作用しており、作成した抗体を用い、これらの分子との内因性の分子間相互作用を確認した。次にCAD活性測定系を構築し、アミノ酸飢餓および添加によるCADの活性の変化を調べたところ、アミノ酸飢餓においてCADの活性が有意に低下することが見出された。CADとmTORのそれぞれの活性の間の直接的な関連性を裏付ける知見は得られてはいないが、mTORの核酸生合成制御機構の関連性を示唆する成果が得られたと思われる。
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (B), Grant-in-Aid for Scientific Research (B), Kobe University, Apr. 2004 - Mar. 2007, Principal investigatorStudy on the Mammalian target of rapamycin in thrombocytepoiesis, wound healing, and hyperlipemiaThe mammalian target of rapamycin (mTOR) is a Ser/Thr protein kinase that plays a crucial role in a nutrient-sensitive signalling pathway that regulates cell growth. TOR signalling is potently inhibited by rapamycin, through the direct binding of a FK506-binding protein 12 (FKBP12)/rapamycin complex to the TOR FRB domain, a segment amino terminal to the kinase catalytic domain. Raptor (regulatory associated protein of mTOR) is a recently identified mTOR binding partner that is essential for mTOR signalling in vivo, and whose binding to mTOR is critical for mTOR-catalyzed substrate phosphorylation in vitro. Here we investigated the stability of endogenous mTOR/raptor complex in response to rapamycin in vivo, and to the direct addition of a FKBP12/rapamycin complex in vitro. We demonstrated that rapamycin inhibits mTOR function, at least in part, by inhibiting the interaction of raptor with mTOR; this action uncouples mTOR from its substrates, and inhibits mTOR signalling without altering mTOR's intrinsic catalytic activity. We showed that heat shock protein 90 (Hsp90) is involved in the regulation of protein translation by facilitating the phosphorylation reaction of eukaryotic initiation factor-4E (eIF4E) binding protein 1 (4E-BP1) and p70 S6 kinase (S6K) catalyzed by the mTOR/raptor complex through the association with raptor, and that the mTOR signaling pathway is a novel target of geldanamycin. We found that the TOS motif has an essential function whereas the RAIP motif has an accessory role in the association with raptor and mTOR-mediated phosphorylation of 4E-BP1 to dissociate it from raptor and release eIF4E in response to amino acid stimulation leading to the control of cell size. The proline-rich Akt substrate of 40 kilodaltons (PRAS40) was identified as a raptor binding protein that is phosphorylated directly by mTOR complex (mTORC) 1 but not mTORC 2 in vitro, predominantly at PRAS40 (Serl 83). We establish PRAS40 as a physiological mTORCl substrate that contains a variant TOS motif Moreover, they indicate that the capacity or ability of raptor to bind endogenous substrates is limiting for the activity of mTORCl in vivo, and is therefore a potential locus of regulation, as suggested by others.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2005 - Mar. 2006, Principal investigatormTORシグナルを介したがん抑制遺伝子TSCによる発がん機構の研究抗がん剤としての薬効が注目されている薬剤ラパマイシンの哺乳動物細胞内の標的タンパク質がmammalian Target of Rapamycin (mTOR)である。mTORはアミノ酸濃度などの細胞が活発に増殖できる環境条件を感知し、細胞成長を制御しているシステムを司る情報伝達系の中枢の分子と考えられている。 一方、遺伝性腎がんラット(Eker Rat)の原因遺伝子であり、がん抑制遺伝子の機能を有する遺伝子Tsc2の産物が、mTORを中枢としたシグナル伝達系の制御に深く関与していることが知られている。この遺伝子はヒト結節性硬化症(Tuberous Sclerosis:TSC)の原因遺伝子と相同であり、その産物TSC2は、別のTSC原因遺伝子Tsc1の産物TSC1と複合体を形成し、低分子量GTP結合タンパク質の一種Rheb(Ras Homolog Enriched in Brain)の機能調節を介し、mTORの機能を制御している。 本研究ではがん抑制遺伝子産物TSC1-TSC2複合体が関与する情報伝達機構を明らかにするために、この複合体と相互作用するタンパク質の探索を試みた。FLAGタグを付加したTSC1およびTSC2をHEK293細胞に発現させ、この複合体と特異的に共精製されるタンパク質を見出し、質量分析法を用いた解析を行ったところ、このタンパク質は約3万2千の分子量を有し、GTPase Activating Protein (GAP)ドメインを備えた機能未知タンパク質であると同定された。この分子は、FLAG-TSC2を単独で細胞内で発現させた際には共精製されないことなどから、直接のBinding PartnerはTSC1であることが示された。またその結合領域は少なくともTSC1コイルドコイル領域のC末端側881-996に限定されることを明らかにした。 本研究によって、TSC1と相互作用するGAPドメインを有した分子としてTSC2とは異なる新規タンパク質が見出され、TSC複合体を介する新たな情報伝達経路の発見につながる知見が得られたものと考える。Competitive research funding
- 科学技術振興機構, 戦略的創造研究推進事業CREST, 「たんぱく質の構造・機能と発現メカニズム」, 神戸大学, Nov. 2002 - Mar. 2006, Coinvestigator細胞成長を司るたんぱく質群の同定と機能解析Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2004 - Mar. 2005, Coinvestigatorアミノ酸情報感知伝達システムを担う分子情報の集積と構築本研究課題は、細胞成長制御シグナリングを司る蛋白質複合体の構成メンバーを同定することを目的として、プロテオミクス的手法によってmammalian target of rapamycin(mTOR)を介したシグナル伝達系を担う新規蛋白質を探索、同定し、その蛋白質のmTORシグナル伝達系における機能を解析することである。昨年に引き続き、申請通り、最近我々が見出した新規蛋白質、mTORシグナル伝達系のスキャフォールド蛋白質raptorに結合する蛋白質の探索、さらにmTORそのものをベイトとした結合蛋白質の探索、同定を試みた。RaptorおよびmTORに、FLAGタグを付加したリコンビナント蛋白質をHEK293細胞に発現させ、このFLAGタグを付加した蛋白質と共精製される蛋白質を、SDS-PAGEによって分離し、質量分析法による同定を試みた。 その結果、有意に結合する蛋白質として数種の候補蛋白質が同定された。そのなかで、今後mTORシグナル伝達系やこの系によってアミノ酸代謝システム、細胞成長を制御するシステムがいかに制御されているのかを解明する重要な手がかりとなりうる40K、120Kの分子量を有する機能未知蛋白質、および80Kの分子量を有するアミノ酸代謝に関与する蛋白質が有意な結合蛋白質として同定された。蛋白質リン酸化酵素であるmTORの基質としては、現在のところ、40Sリボソームの構成蛋白質の一つ、S6蛋白質をリン酸化するp70 S6キナーゼと翻訳開始因子eIF-4Eの活性を制御する4EBP1の2種類のみが知られているが、mTORの新規な基質となる可能性を持った分子も同定された。今後、これらの候補分子の生化学的な解析を進め、mTORシグナル伝達系、そして、細胞成長制御への寄与を明らかにしていきたい。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2004 - Mar. 2005, Coinvestigatorがん抑制遺伝子TSCとGTP結合蛋白Rhebの制御をうけるmTORシグナルの研究ラパマイシンは抗がん剤としての臨床応用が行われている有機化合物である。このラパマイシンの細胞内標的蛋白質は、mTORキナーゼと呼ばれる分子量29万の巨大なSer/Thr蛋白質リン酸化酵素である。mTORキナーゼは、細胞環境中のアミノ酸の濃度バランスを感知するアミノ酸センサーとして機能し、mTOR結合蛋白質raptorを介して、翻訳開始に関わる分子群を制御することにより蛋白質合成を調節している。ヒト遺伝性疾患である結節性硬化症の原因遺伝子TSC1・TSC2複合体がsmall GTP結合蛋白質Rhebを介して、mTORのシグナル伝達系を抑制している。しかしながら、TSC・RhebがmTORシグナル伝達系を抑制する分子基盤は未だ知られていない。本研究では、これらの分子基盤の解明を目指し、プロテオミクス的手法によりmTOR/TSC/Rheb関連蛋白質に結合する分子の候補を探索した。その結果、複数の分子が同定されている。興味深いことに、候補分子の1つは、PKB/Aktのリン酸化モチーフを持ち、アミノ酸依存性にこのモチーフ上のリン酸化が変動することが確認された。この分子の同定は、mTORシグナル系の新たな発見につながる可能性を秘めている。この分子以外の候補分子についても精力的に研究を推進しており、本研究の進展が、抗がん剤であるラパマイシンの作用機序の解明につながるものと期待される。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2003 - Mar. 2005, CoinvestigatorRNA翻訳制御スイッチとして働くラパマイシン標的蛋白mTORシグナルの研究mRNA翻訳抑制作用をもつrapamycinの細胞内標的蛋白質mTOR(mammalian target of rapamycin)は巨大なSer/Thr kinaseである。mTORは、細胞周囲の栄養環境の変化、たとえばアミノ酸濃度の変化を感知して下流分子p70 S6 kinase(p70S6k)などをリン酸化し、蛋白質合成を制御する。Rapamycinは、細胞内でFKBP12と複合体を形成し、この複合体がmTORに結合することによりmTOR機能を阻害するといわれているが、その詳細は不明である。我々は、mTORと複合体を形成する蛋白質raptor(regulatory associated protein of mTOR)を同定した。Raptorは、mTORとその基質であるP70S6kなどの両方に結合し、mTORが基質をリン酸化するための足場を提供するスキャフォールド蛋白質として機能している。本研究では、mTORシグナルの分子基盤の解明を目指し、プロテオミクス的手法によりmTOR/TSC/Rheb関連蛋白質に結合する分子の候補を探索した。その結果、複数の分子が同定されている。興味深いことに、候補分子の1つは、PKB/Aktのリン酸化モチーフを持ち、アミノ酸依存性にこのモチーフ上のリン酸化が変動することが確認された。この分子の同定は、mTORシグナル系の新たな発見につながる可能性を秘めている。この分子以外の候補分子についても精力的に研究を推進しており、本研究の進展が、新たな翻訳調節機構の解明につながるものと期待される。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, Apr. 2003 - Mar. 2005, Principal investigatorMolecular Mining and Functional Analysis of Cell Growth Control SystemThe mammalian target of rapamycin (mTOR) controls cell growth (increase in cell mass or size) in response to availability of nutrient such as amino acids. The mTOR has been known to function as an integrator of larger signaling pathways for cell growth, however, little has been known about members of mTOR signaling. We found the mammalian homolog protein of LST8, which was registered as Similar to G beta-like protein "Gable" in mammalian, is one of components mTOR complex. The mLST8 is a highly conserved 36 kDa protein that consists almost entirely seven WD40 repeats with high sequence similarity to those found in the beta subunit of heterotorimeric G proteins. We identified an enzyme which takes part in pyrimidine biosynthesis as an interacting protein of mLST8 or WD40 domain of raptor. The pyrimidine ring is derived from Gln and Asp, and bicarbonate. This finding suggests that mTOR controls pyrimidine biosynthesis as well as protein synthesis, The TSC1-TSC2 heterodimer (tuberous sclerosis gene products complex) and the small GTPase Rheb (Ras-homolog enriched in brain) have been known as upstream regulator of mTOR. The TSC2 acts as a GTPase activating protein against Rheb. We found another novel GTPase activating protein which interacts to TSC1,as well as TSC2. The molecular size of the novel GTPase activating protein was found to be 32 kDa, and it was shown that the protein interacts to the C-terminal coiled-coil (881-996) of TSC1. We showed that the heat shock protein 90 (Hsp90) was co-purified with raptor. Geldanamycin, a potent inhibitor of Hsp90, disrupted the in vivo binding of Hsp90 to raptor without affecting the association of raptor and mTOR, and suppressed the phosphorylation by mTOR of the downstream translational regulators. It is suggested that the mTOR signaling pathway is a novel target of geldanamycin.Competitive research funding
- サントリー生物有機科学研究所, SUNBOR GRANT, Apr. 2003 - Mar. 2004, Principal investigator細胞環境中のアミノ酸濃度を感知し細胞成長を制御する細胞内情報伝達系を担う蛋白質複合体の機能解析Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2003 - Mar. 2004, Coinvestigator細胞成長システム制御因子分子情報の集積と構築細胞の成長制御にかかわるrapamycinの細胞内標的蛋白質mTOR (mammalian target of rapamycin)は巨大なSer/Thr kinaseである。mTORは、細胞周囲の栄養環境の変化、即ちアミノ酸濃度の変化を感知して下流分子p70 S6 kinase(p70S6k)などをリン酸化し、蛋白質合成を制御する。Rapamycinは、細胞内でFKBP12と複合体を形成し、この複合体がmTORに結合することによりmTOR機能を阻害するといわれているが、その詳細は不明である。我々は、mTORと複合体を形成する蛋白質raptor(regulatory associated protein of mTOR)を同定した。Raptorは、mTORとその基質であるp70S6kなどの両方に結合し、mTORが基質をリン酸化するための足場を提供するスキャフォールド蛋白質として機能している。そこで、mTORとraptorの結合に及ぼすrapamycinの影響を解析した。その結果、以下のことが判明した。(1)In vivoにおけるmTORとraptorの結合は、rapamycin処理により著しく阻害された。(2)FKBP12/rapamycinが結合できないmTOR変異体とraptorの結合は、rapamycin処理によって抑制されなかった。(3)rapamycin処理によりraptorとの結合が阻害されたmTORは、p70S6kなどに対するリン酸化活性が低下していた。(4)In vitroにおいても、FKBP12/rapamycinは直接mTORとraptorの解離を引き起こした。以上より、rapamycinは、mTORとraptorの結合、すなわちmTORが効率よく基質をリン酸化するための足場形成を阻害することにより、mTORの機能を抑制していることが示された。
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, Apr. 2003 - Mar. 2004, Coinvestigator"Research of crosstalk between nutrient sensing mTOR signaling pathway and energy metabolic sensing AMPK"1.The inhibition of mTOR signaling pathway by AMPK We isolated a portion of the γ1 subunit of AMPK, which played a role as an energy metabolic sensor, by yeast two-hybrid screening using mTOR kinase domain as a bait. This result suggests the possibility of the linkage between the nutrient sensing mTOR signaling pathway and the cellular energy metabolic system. Actually the treatments of mammalian cells with AMPK activators inhibit phosphorylations of p70 S6 kinase (p70 S6k) and eukaryotic translational initiation factor 4E binding protein (4EBP1) which function as downstream effectors of mTOR, however a rapamycin-resistant p70 S6k variant is insensitive to AMPK activators. In addition, overexpression of the constitutively active form of AMPK in mammalian cells inhibits phosphorylations of both p70 S6k and 4EBP1. On the other hand, in the dominant negative form of AMPK-over-expressing cells, these inhibitions are restored. These results suggest a possible linkage between AMPK and mTOR signaling. 2.The analysis of a role of mTOR interacting protein raptor as a scaffold protein Both p70 S6k and 4EBP1 have evolutionally conserved TOS (TOR signaling) motif. The mutants of this motif are no longer pbosphorylated by mitogens in cells. We showed that the TOS motif was a binding site of mTOR binding protein raptor. The mutants of the TOS motif cannot bind to raptor and these mutants can be no longer phosphorylated by mTOR in the presence of both mTOR and raptor.
- サントリー生物有機科学研究所, SUNBOR GRANT, Apr. 2002 - Mar. 2003, Principal investigatorアミノ酸バランスを感知し細胞機能を制御する細胞内情報伝達系を担う蛋白質の翻訳後修飾基の解析Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas, Grant-in-Aid for Scientific Research on Priority Areas, Kobe University, Apr. 2002 - Mar. 2003, Coinvestigator哺乳細胞において細胞成長を司るシグナル伝達分子群のプロテオーム解析と機能同定新規mTOR結合蛋白質raptorを同定し、そのcDNAを獲得した。RaptorはmTORと結合し、TORの下流因子4EBP1やp70S6kと結合することも判明した。p70S6kや4EBP1にTOS(conserved TOR signaling)モチーフが存在し、このモチーフに変異を導入すると、p70S6kや4EBP1変異体がin vivoで全くリン酸化を受けないことが報告された。p70S6kおよび4EBP1のTOSモチーフ変異体、はin vitroでraptorと結合せず、かつ、mTORによってもリン酸化されないことが判明した。これらの結果は、raptorはmTORとその基質分子を結合し、反応の足場を与えるscaffold蛋白質として機能していることを示していると考えられた。 raptorに加えてmTORとともに共精製されてくる分子量39kDaのバンドを同定していたが、これがmLST8であることが判明した。mLST8は、7つのWD40リピートから成る蛋白であった。mLST8は、mTORおよびraptorと結合することが確認され、現在その機能解析を進めている。 ESI-Q-TOF-MS型質量分析計を用いてmTOR上に新たなリン酸化部位が存在することを見いだした。このリン酸化部位は細胞環境中のアミノ酸の濃度の増加に伴って上昇するが、ラパマイシンによる阻害は受けず、mTORよりさらに上流にアミノ酸によって活性調節を受けるprotein kinaseの存在が考えられた。 マウスES細胞を用いて、mTORのノックアウトを試みており、ホモノックアウトにより胎生致死となることが確認され、現在conditionalなノックアウト系を確立中である。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, Apr. 2001 - Mar. 2003, CoinvestigatorStudies on molecular mechanism of mTOR signaling that controls various cellular functions in response to amino acid sufficiency.The mammalian target of rapamycin (mTOR) is a protein kinase that controls multiple cellular functions, including cell growth, in response to amino acids and growth factors, in part by regulating the phosphorylation of p70 S6 kinase (p70S6k) and eukaryotic initiation fector 4E-binding protein 1 (4E-BP1). The mechanisms by which mTOR regulates p70S6k and 4E-BP1 in vivo remain incompletely understood. We identified a novel mTOR-binding partner, raptor (regulatory associated protein of mTOR) that also binds p70S6k and 4E-BP1 and is essential for TOR signaling in vivo. We also demonstrated that raptor binds to p70S6k and 4E-BP1 through their respective TOS (conserved TOR signaling) motifs, a short conserved segment previously shown to be required for amino acid- and mTOR-dependent regulation of these mTOR substrates in vivo. A point mutation within the TOS motif of p70S6k or 4E-BP1 known to abolish both amino acid- and mTOR-regulation, selectively abolishes their binding to raptor. This mutation of the TOS motif also eliminates all in vitro mTOR-catalyzed 4E-BP1 phosphorylation and abolishes the raptor-dependent component of mTOR-catalyzed p70S6k phosphorylation in vitro. Raptor does not alter mTOR's intrinsic catalytic activity, but appears to serve as an mTOR scaffold protein whose binding to the TOS motif of mTOR substrates is necessary for effective mTOR-catalyzed phosphorylation in vivo and perhaps for conferring their sensitivity to rapamycin and amino acid sufficiency.Competitive research funding
- 日本学術振興会, 科学研究費助成事業 特定領域研究, 特定領域研究, 神戸大学, 2003 - 2003がん抑制遺伝子TSCに制御されるラパマイシン標的蛋白mTORシグナルの研究抗がん剤として注目されるrapamycinの細胞内標的蛋白質mTOR (mammalian target of rapamycin)は巨大なSer/Thr kinaseである。mTORは、細胞周囲の栄養環境の変化、即ちアミノ酸濃度の変化を感知して下流分子p70 S6 kinase(p70S6k)などをリン酸化し、蛋白質合成を制御する。Rapamycinは、細胞内でFKBP12と複合体を形成し、この複合体がmTORに結合することによりmTOR機能を阻害するといわれているが、その詳細は不明である。我々は、mTORと複合体を形成する蛋白質raptor (regulatory associated protein of mTOR)を同定した。Raptorは、mTORとその基質であるp70S6kなどの両方に結合し、mTORが基質をリン酸化するための足場を提供するスキャフォールド蛋白質として機能している。そこで、mTORとraptorの結合に及ぼすrapamycinの影響を解析した。その結果、以下のことが判明した。(1)In vivoにおけるmTORとraptorの結合は、rapamycin処理により著しく阻害された。(2)FKBP12/rapaillycinが結合できないmTOR変異体とraptorの結合は、rapamycin処理によって抑制されなかった。(3)rapamycin処理によりraptorとの結合が阻害されたmTORは、p70S6kなどに対するリン酸化活性が低下していた。(4)In vitroにおいても、FKBP12/rapamycinは直接mTORとraptorの解離を引き起こした。以上より、rapamycinは、mTORとraptorの結合、すなわちmTORが効率よく基質をリン酸化するための足場形成を阻害することにより、mTORの機能を抑制していることが示された。
- サントリー生物有機科学研究所, SUNBOR GRANT, Apr. 2001 - Mar. 2002, Principal investigatorアミノ酸バランスを感知し、細胞機能を制御する細胞内情報伝達系の分子基盤の解析Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas (C), Grant-in-Aid for Scientific Research on Priority Areas (C), Kobe University, Apr. 2001 - Mar. 2002, Coinvestigator哺乳細胞におけるシグナル伝達機構解明のためのプロテオーム解析の基盤研究哺乳動物でのシグナル伝達機構を網羅的に明らかにするためのプロテオーム的研究手法の基盤研究を行うため、我々が以前より研究を行っている『哺乳細胞において、次世代の免疫抑制剤であるラパマイシンの漂白蛋白mTORキナーゼを解するシグナル伝達系が、細胞を取り巻く環境中のアミノ酸バランスを感知し、細胞増殖因子と共に、細胞機能を制御している』という生命現象を対象とした実験を行った。研究経過を以下に示すと、(1)まず、ラパマイシン処理により変動する蛋白質の同定を、2次元電気泳動法で試み、蛋白質同定に最適な2次元電気泳動法の条件の確立に成功した。が、蛋白質スポットの量の変動の再現性を得るのに困難を極め、結局この方法による変動蛋白質の同定は断念。(2)そこで、mTORに結合する新規蛋白の精製とその同定を試みた。アフィニティーカラム等を用いた蛋白精製により、mTORに結合している可能性のある複数の蛋白の同定に成功。(3)そのうちのp150を質量分析装置を用いたマスフィンガープリンテイング法で分析し、遺伝子を同定。その全長cDNA配列の決定を行い、機能解析のために発現ベクターの作成、抗体の作成を行った。(4)アミノ酸配列の結果から、p150はC末端側にWD-repeat構造を持つ蛋白であることが判明。(5)機能解析の結果、(1)mTORとp150は細胞内で恒常的に結合。(2)p150はmTORのリン酸化酵素活性を4〜5倍上昇させる。(3)p150は翻訳に関わるp70S6kinas6(p70)やeIF-4EBP1(4EBP1)とも結合し、mTORと4量体を形成。(4)p150の過剰発現により、細胞内でp70と4EBP1の活性化/リン酸化が強く阻害される。以上の結果は、p150はmTORに対するscaffold蛋白として機能し、mTORからp70や4EBP1へのシグナル伝達に必須の分子であることを示している。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Exploratory Research, Grant-in-Aid for Exploratory Research, Kobe University, Apr. 2001 - Mar. 2002, Coinvestigator可逆性不死化ヒト肝細胞を用いたプロテオーム解析による不死化機構の研究細胞の不死化は生物学上の大きな問題であり、これから研究を推し進める必要のある重要分野である。初代培養ヒト肝細胞由来で、可逆性に不死化をコントロールできる細胞株NKN-T3細胞を用いて、可逆的に不死化をコントロールし、その時の蛋白質の変動をプロテオーム的アプローチにより網羅的に解析し、未知の不死化機構の解明を試みることが本研究の目的である。研究経過を以下に示すと、(1)NKN-T3細胞由来の蛋白質の同定を、2次元電気泳動法で試み、蛋白質同定に最適な2次元電気泳動法の条件の確立に成功した。が、可逆的に不死化に伴う蛋白質スポットの量の変動の再現性を得るのに困難を極め、結局この方法による変動蛋白質の同定は断念。(2)次に、NKN-T3細胞由来の蛋白質を分画し、SDS-PAGEによる一次元電気泳動での分離した。蛋白質のバンドを切り取りゲル内消化後、ESI-Q-TOF質量分析装置によるマスペプチドフィンガープリンテイング法による解析を行った。この手法により蛋白質を同定することに成功した。現在、NKN-T3細胞を不死化状態から増殖がとまる状態に転換することによって、いかなる蛋白質の発現変動が観察されるか検討中である。(3)また、このNKN-T3細胞は血清の存在、非存在下で肝細胞としての機能を喪失したり、回復したりという性質を有している。そこで、血清の存在、非存在下で細胞を処理し、その抽出物を(2)と同じ手法で解析し、現在変動する蛋白質の解析を行っている。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (B), Grant-in-Aid for Scientific Research (B), Kobe University, Apr. 2000 - Mar. 2002, CoinvestigatorStudies on molecular mechanism of mTOR signaling that controls protein synthesis, cell growth, and cell cycle in response to amino acid sufficiencyThe mammalian target of rapamycin (mTOR) is a protein kinase that controls multiple cellular functions, including cell growth, in response to amino acids and growth factors, in part by regulating the phosphorylation of p70 S6 kinase (p70S6k) and eukaryotic initiation factor 4E-binding protein 1 (4B-BP1). The mechanisms by which mTOR regulates p70S6k and 4B-BP1 in vivo remain incompletely understood. We identified a novel mTOR-binding partner, raptor (regulatory associated protein of mTOR) that also binds p70S6k and 4E-BP1 and is essential for TOR signaling in vivo. We also demonstrated that raptor binds to p70S6k and 4E-BP1 through their respective TOS (conserved TOR signaling) motife, a short conserved segment previously shown to be required for amino acid- and mTOR-dependent regulation of these mTOR substrates in vivo. A point mutation within the TOS motif of p70S6k or 4E-BP1 known to abolish both amino acid- and mTOR-regulation, selectively abolishes their binding to raptor. This mutation of the TOS motif also eliminates all in vitro mTOR-catalyzed 4E-BP1 phosphorylation and abolishes the raptor-dependent component of mTOR-catalyzed p70S6k phosphorylation in vitrv. Raptor does not alter mTOR's intrinsic catalytic activity, but appears to serve as an mTOR scaffold protein whose binding to the TOS motif of mTOR substrates is necessary for effective mTOR-catalyzed phosphorylation in vivo and perhaps for conferring their sensitivity to rapamycin and amino acid sufficiency.Competitive research funding
- 公益信託大阪癌研究者育成基金, 神戸大学, Apr. 2000 - Mar. 2001, Principal investigatorアミノ酸バランスを感知する細胞周期制御システムの解析Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas (C), Grant-in-Aid for Scientific Research on Priority Areas (C), Kobe University, Apr. 2000 - Mar. 2001, Coinvestigatorアミノ酸バランスを感知し、細胞機能を制御するシステムのプロテオーム解析(1)プロテオーム解析系の確立:部分精製蛋白質や哺乳細胞のlysate・細胞分画をSDS-PAGEによる1次元電気泳動、あるいは等電点電気泳動と・SDS-PAGEによる2次元電気泳動で展開し、蛋白を分離、染色を施す。スポットを切り出し消化後、得られたペプチドをハイブリッド型質量分析計(Q-TOF)あるいはMALDI-TOF型質量分析計で解析し、検出された質量の値を用いてデータベースから蛋白を同定するという蛋白質のプロテオーム解析系を確立した。MS/MS法を用いたアミノ酸配列の決定法も確立した。 (2)アミノ酸バランスの変化に伴う蛋白発現変動のプロテオーム解析:哺乳細胞をアミノ酸を含む、または含まない培養液で処理後、上記の要領でプロテオーム解析を行なった。しかし、細胞のlysateや細胞分画をサンプルとした場合、画像解析システムで量的変動がみられるスポットはごくわずかであり、また再現性に問題があり、改善が必要と思われた。 (3)アミノ酸バランスの変化に伴うmTORの翻訳後修飾の解析:リン酸化されたmTORを消化し、質量分析計で分析。質量変化に基づき複数のリン酸化部位を同定した。このリン酸化部位に点変異を導入し、mTOR機能に及ぼす影響を検討中である。 (4)今後の展望 哺乳細胞のlysateを2次元電気泳動で分離し、その量的変動を捕らえることはかなり困難であると思われる。今後は、全体の蛋白を相手にするのではなく、ある基準を決定し、それに合致した蛋白群・翻訳後修飾にfocusし、解析法を考える必要性がある。たとえば、アミノ酸変動に伴うリン酸化蛋白質にfocusした解析などを開発していく予定である。Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research on Priority Areas (C), Grant-in-Aid for Scientific Research on Priority Areas (C), Kobe University, Apr. 2000 - Mar. 2001, CoinvestigatorG1期における細胞成長・細胞周期を制御する分子に着目した新たながん治療法の研究(1)免疫抑制剤ラパマイシンの細胞内標的蛋白mTORがアミノ酸バランスを感知し、蛋白合成系・細胞成長・細胞周期を制御する中心分子である事を示すため、高率にhomologous recombinationを起こすチキンB細胞DT40を用い、まず外来性のラットmTORをテトラサイクリンで発現を制御する系を作製。その細胞を使って、mTORのknockout細胞を作成しつつある。 (2)アミノ酸のなかでもロイシンが、最も強くmTORの情報伝達系を活性化し、ロイシンのL体、アミノ基、側鎖が重要。ベータアラニンとリジンからなるmulti-antigen peptide(MAP)中のリジンのアルファ・イプシロンアミノ基に、8つのロイシン(L体)をカルボキシル基を介して結合させ、Leu8-MAPを合成。これは、分子量約2000で、細胞膜を通過できない。ラット肝癌細胞H4IIEをLeu8-MAPで刺激すると、mTOR下流のp70S6キナーゼが活性化される。この時Leu8-MAPの分解はほとんど観察されず、Leu8-MAPが細胞表面から作用したと思われた。 (3)ロイシン誘導体中にロイシンによるp70S6キナーゼの活性化を阻害する化合物を発見。このロイシン誘導体の細胞増殖に対する効果は、ラパマイシン感受性ヒトT細胞であるJurkat細胞において、血清存在下で、細胞数増加を抑制、G1期で停止、サイクリンキナーゼ阻害因子p27Kip1の発現量の増加とretinoblastoma蛋白のリン酸化の低下を誘導。 (4)mTORを介するシグナル系に関与する新規シグナル伝達分子の探索を行なうため、yeast two hybrid法と生化学的手法を用いた。mTORに対するモノクロナール抗体を作製し、この抗体のアフィニティカラムで、mTORを精製、共に精製されてくる蛋白を発見。現在、解析を行なっている。Competitive research funding
- 平成8年度保健医療分野における基礎研究推進事業, Apr. 1996 - Sep. 1997, Coinvestigator大腸菌O157などの新興感染症の予防と治療を目的とした病原性の分子機構解明Competitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Encouragement of Young Scientists (A), Grant-in-Aid for Encouragement of Young Scientists (A), 国立小児病院, Apr. 1996 - Mar. 1997, Principal investigatorエルシニア菌由来スーパー抗原の活性発現領域の解析我々はYersinia pseudotuberculosisが産生する新規なスーパー抗原(YPM)を見いだし、これを精製、その一次構造を明らかにした。YPMは既知の細菌性スーパー抗原のみならず、一次構造の知られているどのタンパク質とも相同性がない全く新規なタンパク質であった。 本研究ではYPMに加えてエルシニア菌由来の新規なスーパー抗原YPMbを見いだし、その精製、さらにこれをコードする遺伝子の塩基配列を決定することによってその一次構造および生物学的性質を明らかにした。YPMbと既知のYPM(YPMa)の前駆体蛋白質間の相同性はアミノ酸レベルで82%、遺伝子レベルで90%であった。YPMb成熟蛋白質を構成する130残基のアミノ酸残基のうちYPMaと相同な残基は108残基で、アミノ酸レベルの相同性は83%であった。以上の結果から、YPMbは最小活性発現量およびVβレパトリ-の生物学的性質は既知のYPM分子とは同一ながらアミノ酸配列の異なるバリアント分子であることが明かとなった。決定された塩基配列からYPMbのN末端側とC末端側は比較的良く保存されているが、中央付近に多くの置換が見られた。このことから、YPMのアミノ酸配列において、N末端領域やC末端領域に比べて、分子中央部はYPMの機能においてその重要性が低いことが示唆される。 本研究ではさらに、YPMa部分ペプチドを化学合成し、YPMaによって誘起されるリンパ球増殖活性に対するそれらの阻害能を調べることによってさらにYPMの構造と機能との相関を検討した。7種の部分ペプチドのうちN末端側23残基からなるペプチドだけが特異的な阻害能を有していた。IC50は約50μMであった。YPMのアミノ酸配列において、少なくとも23残基までのN末端側領域がリンパ球増殖活性に重要であることが明かとなった。このことはYPMaとYPMb分子間のN末端側アミノ酸配列における高い相同性からも強く示唆される。Competitive research funding
- 財団法人日本科学協会, 笹川科学研究助成金, Apr. 1995 - Mar. 1996, Principal investigatorグラム陰性桿菌由来スーパー抗原の機能構造の解析Competitive research funding
- 財団法人神奈川科学技術アカデミー, 研究助成事業, 研究助成第1段階, Apr. 1995 - Mar. 1996, Principal investigatorグラム陰性桿菌スーパー抗原の構造機能相関Competitive research funding
- 厚生省, 小児医療共同研究, 国立小児病院, Apr. 1995 - Mar. 1996, Coinvestigator細菌感染に続発する小児難治性疾患の全国規模における臨床医学的研究
- 文部省, 科学研究費補助金(特別研究員奨励費), Apr. 1992 - Sep. 1993, Principal investigator質量分析法による膜結合性グアニル酸シクラーゼ成熟タンパク質の活性型一次構造の解析Competitive research funding
- Lecturer, 09 May 2025 - 09 May 2025丹波市立和田小学校出前授業
- 02 Dec. 2024 - 15 Jan. 2025, オンデマンド第53回質量分析講習会
- 11 Jul. 2024 - 30 Sep. 2024, 大阪大学豊中キャンパス全学教育推進機構DAICEL Studio(スタジオA)およびオンデマンド第52回質量分析講習会
- 第51回質量分析講習会, 13 Nov. 2023 - 14 Nov. 2023第51回質量分析講習会
- 第50回質量分析講習会, 29 May 2023 - 14 Jul. 2023第50回質量分析講習会
- 第49回質量分析講習会, 22 Nov. 2022 - 13 Jan. 2023第49回質量分析講習会
- 第48回質量分析講習会, 01 Jul. 2022 - 01 Aug. 2022第48回質量分析講習会
- Lecturer, 研修会「いきいきライフセミナー」, 22 Jan. 2022 - 22 Jan. 2022加西市老人クラブ連合会研修会 講師
- 第47回質量分析講習会, 01 Nov. 2021 - 30 Nov. 2021第47回質量分析講習会
- Coverage cooperation, ちゃちゃ入れマンデー, 22 Jun. 2021 - 22 Jun. 2021, Media「ちゃちゃ入れマンデー」 取材協力
- 第43回質量分析講習会, 19 Jun. 2019 - 20 Jun. 2019, LiSE川崎生命科学・環境研究センター第43回質量分析講習会
- 第42回質量分析講習会, 20 Jun. 2018 - 21 Jun. 2018, 公益財団法人微生物化学研究会微生物化学研究所第42回質量分析講習会
- Chief, 01 Apr. 2013 - 31 Mar. 2015, Researchers日本質量分析学会 会誌編集委員長
- 第33回質量分析講習会, 28 May 2013 - 29 May 2013, 千里ライフサイエンスセンター第33回質量分析講習会
- 第32回質量分析講習会, 13 Nov. 2012 - 14 Nov. 2012, 千里ライフサイエンスセンター第32回質量分析講習会
- 第31回質量分析講習会, 04 Jun. 2012 - 05 Jun. 2012, 千里ライフサイエンスセンター第31回質量分析講習会
- 第30回質量分析講習会, 05 Dec. 2011 - 06 Dec. 2011, 千里ライフサイエンスセンター第30回質量分析講習会
- Chief, 01 Apr. 2005 - 31 Mar. 2009, 日本質量分析学会, Researchers日本質量分析学会 会誌編集委員長
- Lecturer, 第39回千里ライフサイエンス技術講習会, 28 Jul. 2005 - 29 Jul. 2005, Researchersプロテオミクス技術講習会「MALDI,ESI,MS/MS,ナノLC,データ解析」
- 第23回技術講習会「質量分析による蛋白質同定法」, 05 Sep. 2004 - 08 Sep. 2004, 千里ライフサイエンスセンター、島津製作所, Researchers平成16年度日本細菌学会技術講習会
- Organizing member, Feb. 1997 - Sep. 1997ベロ毒素吸着剤「TAK-751S」治験実施班班員
- Lecturer, The South East Asian Medical Information Center (SEAMIC) National Group Training Course on New Technique for the Identification of the Pathogenic E. coli and New Strain of V. cholera, 10 Mar. 1997 - 14 Mar. 1997, National Institute for Health Research & Development (NIHRD), Jakarta, Indonesia, ResearchersThe South East Asian Medical Information Center (SEAMIC) National Group Training Course on New Technique for the Identification of the Pathogenic E. coli and New Strain of V. cholera
- Myself, 関西テレビ, ちゃちゃ入れマンデー, Jun. 2021写真およびデータ提供Media report
- 小学館, 「大丈夫」7月号, Jul. 1997写真「病原性大腸菌O157の増殖」Paper
- Myself, 朝日新聞社, 朝日新聞報道写真集’97, 30 Jan. 1997写真「病原性大腸菌O157の増殖」Paper
- Other than myself, 読売新聞, 08 Nov. 1996, 東京朝刊Paper
- Myself, 朝日新聞朝刊, 25 Aug. 1996写真「病原性大腸菌O157の増殖」Paper
- 第6回日本質量分析学会スペクトルデータ部会/第8回東北談話会共催シンポジウム15 Mar. 2025 - 15 Mar. 2025, ZoomCompetition etc
- 第27回日本質量分析学会中部談話会第27回日本質量分析学会中部談話会22 Nov. 2024 - 22 Nov. 2024, 名古屋大学Academic society etc
- 第49回BMSコンファレンス18 Jul. 2023 - 20 Jul. 2023, Hotel & Resorts BEPPWANAcademic society etc
- 第3回日本質量分析学会東北談話会・第17回日本質量分析学会中部談話会09 Dec. 2020 - 09 Dec. 2020, ZoomAcademic society etc
- 第37回BMSコンファレンス第37回BMSコンファレンス07 Jul. 2010 - 10 Jul. 2010, 沖縄残波岬ロイヤルホテルAcademic society etc
- 第118回質量分析関西談話会第118回質量分析関西談話会26 Sep. 2009 - 26 Sep. 2009, 大阪府立大学中之島サテライトAcademic society etc
- 第57回質量分析総合討論会第57回質量分析総合討論会13 May 2009 - 15 May 2009, 大阪国際交流センターAcademic society etc
- 第34回BMSコンファレンス第34回BMSコンファレンス08 Jul. 2007 - 11 Jul. 2007, 鳥羽シーサイドホテルAcademic society etc
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