野村 渉WATARU NOMURA

Last Updated :2024/07/05

所属・職名
大学院医系科学研究科（薬）　教授
メールアドレス
wnomurahiroshima-u.ac.jp
自己紹介
研究では主にゲノム編集技術、タンパク質工学、蛍光イメージング技術に興味を持ち、これまでにないような機能性タンパク質の創製やそれらを活用した新しいスクリーニング技術、研究手法の開発、などを目的としています。ゲノム編集技術は様々な生物に利用できる遺伝子書き換える技術で、医療や農畜産業など様々な産業での応用が期待されています。より正確で安全性の高い手法を開発することは応用の幅も拡げることにつながると期待しています。

基本情報

主な職歴

  • 2002年04月, 2005年03月, 日本学術振興会, 特別研究員
  • 2005年04月, 2007年07月, スクリプス研究所, 博士研究員
  • 2007年08月, 2011年12月, 東京医科歯科大学, 助教
  • 2012年01月, 2013年03月, 東京医科歯科大学, 講師
  • 2013年04月, 2019年03月, 東京医科歯科大学, 准教授
  • 2019年04月, 広島大学, 大学院医系科学研究科, 教授

学歴

  • 京都大学, 薬学研究科, 生命薬科学専攻博士後期課程, 日本, 2002年04月, 2005年03月
  • 京都大学, 薬学研究科, 生命薬科学専攻修士課程, 日本, 2000年04月, 2002年03月
  • 京都大学, 薬学部, 薬学科, 日本, 1996年04月, 2000年03月

学位

  • 博士（薬学）　(京都大学)

教育活動

授業担当

  1. 2024年, 学部専門, ２ターム, 機能形態学
  2. 2024年, 学部専門, ２ターム, 生化学IV
  3. 2024年, 学部専門, ３ターム, 薬学概論
  4. 2024年, 学部専門, セメスター（前期）, 薬学研究方法論演習Ａ
  5. 2024年, 学部専門, セメスター（後期）, 薬学研究方法論演習Ｂ
  6. 2024年, 学部専門, セメスター（前期）, 細胞薬理学演習
  7. 2024年, 学部専門, ２ターム, 生理化学
  8. 2024年, 学部専門, ３ターム, 日本薬局方演習
  9. 2024年, 学部専門, セメスター（後期）, 生物化学実習
  10. 2024年, 学部専門, 通年, 基礎研究I
  11. 2024年, 学部専門, 通年, 基礎研究II
  12. 2024年, 学部専門, セメスター（後期）, 基礎研究III
  13. 2024年, 学部専門, 通年, 臨床研究I
  14. 2024年, 学部専門, 通年, 臨床研究II
  15. 2024年, 学部専門, 通年, 臨床研究III
  16. 2024年, 博士課程・博士課程後期, セメスター（前期）, 生理化学特別演習
  17. 2024年, 博士課程・博士課程後期, セメスター（後期）, 生理化学特別演習
  18. 2024年, 博士課程・博士課程後期, セメスター（前期）, 生理化学特別研究
  19. 2024年, 博士課程・博士課程後期, セメスター（後期）, 生理化学特別研究
  20. 2024年, 修士課程・博士課程前期, セメスター（前期）, 薬科学特論
  21. 2024年, 博士課程・博士課程後期, セメスター（前期）, 薬科学特講
  22. 2024年, 修士課程・博士課程前期, セメスター（前期）, 細胞内情報伝達学特論演習
  23. 2024年, 修士課程・博士課程前期, セメスター（後期）, 細胞内情報伝達学特論演習
  24. 2024年, 修士課程・博士課程前期, セメスター（前期）, 細胞内情報伝達学特別研究
  25. 2024年, 修士課程・博士課程前期, セメスター（後期）, 細胞内情報伝達学特別研究
  26. 2024年, 博士課程・博士課程後期, セメスター（前期）, 生理化学特別演習
  27. 2024年, 博士課程・博士課程後期, セメスター（後期）, 生理化学特別演習
  28. 2024年, 博士課程・博士課程後期, セメスター（前期）, 生理化学特別研究
  29. 2024年, 博士課程・博士課程後期, セメスター（後期）, 生理化学特別研究
  30. 2024年, 博士課程・博士課程後期, ３ターム, ゲノム編集先端研究特論A

研究活動

学術論文（★は代表的な論文）

  1. SpCas9-HF1 enhances accuracy of cell cycle-dependent genome editing by increasing HDR efficiency, and by reducing off-target effects and indel rates, MOLECULAR THERAPY NUCLEIC ACIDS, 35巻, 1号, 20240312
    DOIを用いた論文検索結果へのリンク
  2. Development of the 8-aza-3-bromo-7-hydroxycoumarin-4-ylmethyl group as a new entry of photolabile protecting groups, Tetrahedron, 70巻, 29号, pp. 4400-4404, 20140722
  3. Development of a fluoride-responsive amide bond cleavage device that is potentially applicable to a traceable linker, Tetrahedron, 70巻, 34号, pp. 5122-5127, 20140826
  4. Development of site-specific DNA methylase for epigenetic regulation of gene expression, Seikagaku, 82巻, 5号, pp. 393-397, 20101201
  5. Significant effect of linker sequence on DNA recognition by multi-zinc finger protein, Biochemical and Biophysical Research Communications, 282巻, 4号, pp. 1001-1007, 20010101
  6. Multiconnection of identical zinc finger: Implication for DNA binding affinity and unit modulation of the three zinc finger domain, Biochemistry, 40巻, 9号, pp. 2932-2941, 20010306
  7. The history of genome editing: advances from the interface of chemistry & biology, CHEMICAL COMMUNICATIONS, 59巻, 50号, pp. 7676-7684, 20230620
    DOIを用いた論文検索結果へのリンク
  8. Interconversion between serine and aspartic acid in the alpha helix of the N-terminal zinc finger of Sp1: implication for general recognition code and for design of novel zinc finger peptide recognizing complementary strand., Biochemistry, 41巻, 28号, 2002
  9. Influence of TFIIIA-type linker at the N- or C-terminal of nine-zinc finger protein on DNA-binding site., Biochemical and biophysical research communications, 300巻, 1号, 2003
  10. Effects of length and position of an extended linker on sequence-selective DNA recognition of zinc finger peptides., Biochemistry, 42巻, 50号, 2003
  11. Effects of linking 15-zinc finger domains on DNA binding specificity and multiple DNA binding modes., Bioorganic & medicinal chemistry letters, 15巻, 9号, 2005
  12. Design and synthesis of artificial zinc finger proteins., Methods in molecular biology (Clifton, N.J.), 352巻, 2007
  13. In vivo site-specific DNA methylation with a designed sequence-enabled DNA methylase., Journal of the American Chemical Society, 129巻, 28号, 2007
  14. Fluorophore labeling enables imaging and evaluation of specific CXCR4-ligand interaction at the cell membrane for fluorescence-based screening., Bioconjugate chemistry, 19巻, 9号, 2008
  15. Structure-activity relationship study of CXCR4 antagonists bearing the cyclic pentapeptide scaffold: identification of the new pharmacophore., Organic & biomolecular chemistry, 6巻, 23号, 2008
  16. Synthesis of protein kinase Cdelta C1b domain by native chemical ligation methodology and characterization of its folding and ligand binding., Journal of peptide science : an official publication of the European Peptide Society, 15巻, 10号, 2009
  17. Structure-activity relationship study on artificial CXCR4 ligands possessing the cyclic pentapeptide scaffold: the exploration of amino acid residues of pentapeptides by substitutions of several aromatic amino acids., Organic & biomolecular chemistry, 7巻, 18号, 2009
  18. Exploratory studies on development of the chemokine receptor CXCR4 antagonists toward downsizing., Perspectives in medicinal chemistry, 2巻, 2008
  19. Fluorogenically active leucine zipper peptides as tag-probe pairs for protein imaging in living cells., Angewandte Chemie (International ed. in English), 48巻, 48号, 2009
  20. CD4 mimics targeting the mechanism of HIV entry., Bioorganic & medicinal chemistry letters, 20巻, 1号, 2010
  21. Remodeling of dynamic structures of HIV-1 envelope proteins leads to synthetic antigen molecules inducing neutralizing antibodies., Bioconjugate chemistry, 21巻, 4号, 2010
  22. [Development of site-specific DNA methylase for epigenetic regulation of gene expression]., Seikagaku. The Journal of Japanese Biochemical Society, 82巻, 5号, 2010
  23. Development of crosslink-type tag-probe pairs for fluorescent imaging of proteins., Biopolymers, 94巻, 6号, 2010
  24. Peptide HIV-1 integrase inhibitors from HIV-1 gene products., Journal of medicinal chemistry, 53巻, 14号, 2010
  25. Peptidic HIV integrase inhibitors derived from HIV gene products: structure-activity relationship studies., Bioorganic & medicinal chemistry, 18巻, 18号, 2010
  26. CD4 mimics targeting the HIV entry mechanism and their hybrid molecules with a CXCR4 antagonist., Bioorganic & medicinal chemistry letters, 20巻, 19号, 2010
  27. Bivalent ligands of CXCR4 with rigid linkers for elucidation of the dimerization state in cells., Journal of the American Chemical Society, 132巻, 45号, 2010
  28. Fluorescent-responsive synthetic C1b domains of protein kinase Cδ as reporters of specific high-affinity ligand binding., Bioconjugate chemistry, 22巻, 1号, 2011
  29. Azamacrocyclic metal complexes as CXCR4 antagonists., ChemMedChem, 6巻, 5号, 2011
  30. Intense blue fluorescence in a leucine zipper assembly., Chembiochem : a European journal of chemical biology, 12巻, 5号, 2011
  31. Fluorescence-quenching screening of protein kinase C ligands with an environmentally sensitive fluorophore., Bioconjugate chemistry, 22巻, 5号, 2011
  32. Small molecular CD4 mimics as HIV entry inhibitors., Bioorganic & medicinal chemistry, 19巻, 22号, 2011
  33. Synthetic caged DAG-lactones for photochemically controlled activation of protein kinase C., Chembiochem : a European journal of chemical biology, 12巻, 4号, 2011
  34. A synthetic C34 trimer of HIV-1 gp41 shows significant increase in inhibition potency., ChemMedChem, 7巻, 2号, 2012
  35. Conjugation of cell-penetrating peptides leads to identification of anti-HIV peptides from matrix proteins., Bioorganic & medicinal chemistry, 20巻, 4号, 2012
  36. Effects of DNA binding of the zinc finger and linkers for domain fusion on the catalytic activity of sequence-specific chimeric recombinases determined by a facile fluorescent system., Biochemistry, 51巻, 7号, 2012
  37. Evaluation of a synthetic C34 trimer of HIV-1 gp41 as AIDS vaccines., Bioorganic & medicinal chemistry, 20巻, 10号, 2012
  38. Pharmacophore-based small molecule CXCR4 ligands., Bioorganic & medicinal chemistry letters, 22巻, 12号, 2012
  39. The successes and failures of HIV drug discovery., Expert opinion on drug discovery, 6巻, 10号, 2011
  40. Low-molecular-weight CXCR4 ligands with variable spacers., ChemMedChem, 8巻, 1号, 2013
  41. A future perspective on the development of chemokine receptor CXCR4 antagonists., Expert opinion on drug discovery, 3巻, 10号, 2008
  42. CD4 mimics as HIV entry inhibitors: lead optimization studies of the aromatic substituents., Bioorganic & medicinal chemistry, 21巻, 9号, 2013
  43. Multimerized CHR-derived peptides as HIV-1 fusion inhibitors., Bioorganic & medicinal chemistry, 21巻, 15号, 2013
  44. Peptide-based ligand screening and functional analysis of protein kinase C., Biopolymers, 100巻, 6号, 2013
  45. Cell-permeable stapled peptides based on HIV-1 integrase inhibitors derived from HIV-1 gene products., ACS chemical biology, 8巻, 10号, 2013
  46. Anti-HIV-1 peptide derivatives based on the HIV-1 Co-receptor CXCR4., ChemMedChem, 8巻, 10号, 2013
  47. CXCR4-derived synthetic peptides inducing anti-HIV-1 antibodies., Bioorganic & medicinal chemistry, 21巻, 22号, 2013
  48. A CD4 mimic as an HIV entry inhibitor: pharmacokinetics., Bioorganic & medicinal chemistry, 21巻, 24号, 2013
  49. Development of a traceable linker containing a thiol-responsive amino acid for the enrichment and selective labelling of target proteins., Organic & biomolecular chemistry, 12巻, 23号, 2014
  50. Screening for protein kinase C ligands using fluorescence resonance energy transfer., Chemical & pharmaceutical bulletin, 62巻, 10号, 2014
  51. [Chemical biology for pharmaceutical science--integrative approaches for elucidation of biological phenomena]., Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 135巻, 3号, 2015
  52. [Application and potential of genome engineering by artificial enzymes]., Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 135巻, 3号, 2015
  53. An in-cell fluorogenic Tag-probe system for protein dynamics imaging enabled by cell-penetrating peptides., Bioconjugate chemistry, 26巻, 6号, 2015
  54. Anti-HIV screening for cell-penetrating peptides using chloroquine and identification of anti-HIV peptides derived from matrix proteins., Bioorganic & medicinal chemistry, 23巻, 15号, 2015
  55. Trivalent ligands for CXCR4 bearing polyproline linkers show specific recognition for cells with increased CXCR4 expression., Organic & biomolecular chemistry, 13巻, 32号, 2015
  56. Exploration of labeling by near infrared dyes of the polyproline linker for bivalent-type CXCR4 ligands., Bioorganic & medicinal chemistry, 23巻, 21号, 2015
  57. Utilization of the Heavy Atom Effect for the Development of a Photosensitive 8-Azacoumarin-Type Photolabile Protecting Group., Organic letters, 17巻, 21号, 2015
  58. Multimerized HIV-gp41-derived peptides as fusion inhibitors and vaccines., Biopolymers, 106巻, 4号, 2016
  59. A minimally cytotoxic CD4 mimic as an HIV entry inhibitor., Bioorganic & medicinal chemistry letters, 26巻, 2号, 2016
  60. Small-Molecule CD4 Mimics Containing Mono-cyclohexyl Moieties as HIV Entry Inhibitors., ChemMedChem, 11巻, 8号, 2016
  61. Functional evaluation of fluorescein-labeled derivatives of a peptide inhibitor of the EGF receptor dimerization., Bioorganic & medicinal chemistry, 24巻, 16号, 2016
  62. Development of anti-HIV peptides based on a viral capsid protein., Biopolymers, 108巻, 1号, 2017
  63. Bivalent 14-mer peptide ligands of CXCR4 with polyproline linkers with anti-chemotactic activity against Jurkat cells., Journal of peptide science : an official publication of the European Peptide Society, 23巻, 7-8号, 2017
  64. Microwave-Assisted Synthesis of Azacoumarin Fluorophores and the Fluorescence Characterization., The Journal of organic chemistry, 82巻, 5号, 2017
  65. Synthesis and Evaluation of Dimeric Derivatives of Diacylglycerol-Lactones as Protein Kinase C Ligands., Bioconjugate chemistry, 28巻, 8号, 2017
  66. Synthesis of a Chloroalkene Dipeptide Isostere-Containing Peptidomimetic and Its Biological Application., ACS medicinal chemistry letters, 9巻, 1号, 2018
  67. [ZIP tag-probe system: A fluorescence imaging tool for intercellular proteins]., Seikagaku. The Journal of Japanese Biochemical Society, 89巻, 1号, 2017
  68. Delivery of a Proapoptotic Peptide to EGFR-Positive Cancer Cells by a Cyclic Peptide Mimicking the Dimerization Arm Structure of EGFR., Bioconjugate chemistry, 29巻, 6号, 2018
  69. Development of Toolboxes for Precision Genome/Epigenome Editing and Imaging of Epigenetics., Chemical record (New York, N.Y.), 18巻, 12号, 2018
  70. Efficient and Orthogonal Transcription Regulation by Chemically Inducible Artificial Transcription Factors., Biochemistry, 57巻, 45号, 2018
  71. Inhibition of EGFR Activation by Bivalent Ligands Based on a Cyclic Peptide Mimicking the Dimerization Arm Structure of EGFR., Chemical & pharmaceutical bulletin, 66巻, 11号, 2018
  72. Design, synthesis and biological evaluation of low molecular weight CXCR4 ligands., Bioorganic & medicinal chemistry, 27巻, 6号, 2019
  73. Dimeric C34 Derivatives Linked through Disulfide Bridges as New HIV-1 Fusion Inhibitors., Chembiochem : a European journal of chemical biology, 20巻, 16号, 2019
  74. Introducing "Future of Biochemistry 2020: The Asia-Pacific Issue", BIOCHEMISTRY, 59巻, 1号, pp. 1-7, 2020
  75. ★, TALEN-Based Chemically Inducible, Dimerization-Dependent, Sequence-Specific Nucleases, Biochemistry, 59巻, 2号, pp. 197-204, 20200121
  76. Synthesis of hydrophilic caged DAG-lactones for chemical biology applications, Organic and Biomolecular Chemistry, 18巻, 22号, pp. 4217-4223, 20200614
  77. Development of a NanoBRET-Based Sensitive Screening Method for CXCR4 Ligands, BIOCONJUGATE CHEMISTRY, 30巻, 5号, pp. 1442-1450, 2019
  78. A minimally cytotoxic CD4 mimic as an HIV entry inhibitor, Bioorganic and Medicinal Chemistry Letters, 26巻, 2号, pp. 397-400, 20160115
  79. Small-Molecule CD4 Mimics Containing Mono-cyclohexyl Moieties as HIV Entry Inhibitors, ChemMedChem, 11巻, 8号, pp. 940-946, 20160419
  80. Multimerized HIV-gp41-derived peptides as fusion inhibitors and vaccines, Biopolymers, pp. 622-628, 20161104
  81. Development of anti-HIV peptides based on a viral capsid protein, Biopolymers, 108巻, 1号, 20170101
  82. Microwave-Assisted Synthesis of Azacoumarin Fluorophores and the Fluorescence Characterization, Journal of Organic Chemistry, 82巻, 5号, pp. 2739-2744, 20170303
  83. Bivalent 14-mer peptide ligands of CXCR4 with polyproline linkers with anti-chemotactic activity against Jurkat cells, Journal of Peptide Science, 23巻, 7-8号, pp. 574-580, 20170701
  84. Synthesis and Evaluation of Dimeric Derivatives of Diacylglycerol-Lactones as Protein Kinase C Ligands, Bioconjugate Chemistry, 28巻, 8号, pp. 2135-2144, 20170816
  85. Creation of functional molecules based on biomolecular interactions; development toward chemical biology, Yakugaku Zasshi, 137巻, 10号, pp. 1223-1231, 20170101
  86. ZIP tag-probe system: A fluorescence imaging tool for intercellular proteins, Seikagaku, 89巻, 1号, pp. 115-120, 20170101
  87. Synthesis of a Chloroalkene Dipeptide Isostere-Containing Peptidomimetic and Its Biological Application, ACS Medicinal Chemistry Letters, 9巻, 1号, pp. 7-11, 20180111
  88. Delivery of a Proapoptotic Peptide to EGFR-Positive Cancer Cells by a Cyclic Peptide Mimicking the Dimerization Arm Structure of EGFR, Bioconjugate Chemistry, 29巻, 6号, pp. 2050-2057, 20180620
  89. Development of Toolboxes for Precision Genome/Epigenome Editing and Imaging of Epigenetics, Chemical Record, 18巻, 12号, pp. 1717-1726, 20181201
  90. Inhibition of EGFR activation by bivalent ligands based on a cyclic peptide mimicking the dimerization arm structure of EGFR, Chemical and Pharmaceutical Bulletin, 66巻, 11号, pp. 1083-1089, 20180101
  91. Efficient and Orthogonal Transcription Regulation by Chemically Inducible Artificial Transcription Factors, Biochemistry, 57巻, 45号, pp. 6452-6459, 20181113
  92. Benzolactam-related compounds promote apoptosis of HIV-infected human cells via protein kinase C–induced HIV latency reversal, Journal of Biological Chemistry, 294巻, 1号, pp. 116-129, 20190104
  93. Design, synthesis and biological evaluation of low molecular weight CXCR4 ligands, Bioorganic and Medicinal Chemistry, 27巻, 6号, pp. 1130-1138, 20190315
  94. Development of a NanoBRET-based sensitive screening method for CXCR4 ligands, Bioconjugate Chemistry, 30巻, 5号, pp. 1442-1450, 20190515
  95. Dimeric C34 Derivatives Linked through Disulfide Bridges as New HIV-1 Fusion Inhibitors, ChemBioChem, 20巻, 16号, pp. 2101-2108, 20190101
  96. ★, A cell cycle-dependent CRISPR-Cas9 activation system based on an anti-CRISPR protein shows improved genome editing accuracy, Communications Biology, 3巻, 1号, 20201201
  97. Discovery of a Macropinocytosis-Inducing Peptide Potentiated by Medium-Mediated Intramolecular Disulfide Formation, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 60巻, 21号, pp. 11928-11936, 20210517
    DOIを用いた論文検索結果へのリンク
  98. ★, Molecular Switch Engineering for Precise Genome Editing, BIOCONJUGATE CHEMISTRY, 32巻, 4号, pp. 639-648, 20210421
    DOIを用いた論文検索結果へのリンク
  99. Fluorescence resonance energy transfer-based screening for protein kinase C ligands using 6-methoxynaphthalene-labeled 1,2-diacylglycerol-lactones, ORGANIC & BIOMOLECULAR CHEMISTRY, 19巻, 38号, pp. 8264-8271, 20211006
    DOIを用いた論文検索結果へのリンク

著書等出版物

  1. 2022年05月12日, BIOINDUSTRY【特集】ペプチド医薬の最新動向 ～広い観点からのペプチド創薬科学～, HIV-1阻害剤・腫瘍認識プローブとしてのケモカイン受容体リガンド, CMC出版, 2022年, 05, 単行本（学術書）, 共著, 日本語, 野村渉、玉村啓和

受賞

  1. 2023年01月28日, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会 2022年度学生発表奨励賞, 公益社団法人日本薬学会中国四国支部支部長, CRISPRa/iによる Anti-CRISPR/CRISPR Cas9 相互作用解析
  2. 2016年09月17日, 日本薬学会関東支部奨励賞, 日本薬学会関東支部, 生体分子間相互作用を基盤とする機能分子の創製とケミカルバイオロジーへの展開
  3. 2013年11月08日, 日本ペプチド学会奨励賞, 日本ペプチド学会, ペプチド性化合物の分子間相互作用を基盤としたプローブおよび阻害剤の創製