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2013 Fiscal Year Final Research Report

Molecular mechanisms of permeability transition revealed using quantitative proteomic analysis

Research Project

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Project/Area Number 24790076
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Research InstitutionThe University of Tokushima

Principal Investigator

YAMAMOTO Takenori  徳島大学, 疾患プロテオゲノム研究センター, 講師 (80457324)

Project Period (FY) 2012-04-01 – 2014-03-31
Keywordsミトコンドリア / 透過性遷移 / プロテオミクス
Research Abstract

Mitochondrial permeability transition triggers subsequent steps of apoptosis. To understand the molecular mechanisms of permeability transition, we here performed the quantitative proteomic analysis to identify the regulatory proteins for permeability transition. As a result, we found some candidate proteins, which were oxidized when a permeability transition inducer was added to isolated mitochondria. We will examine whether the proteins are related to the regulation of permeability transition.

  • Research Products

    (9 results)

All 2014 2013 2012

All Journal Article (6 results) (of which Peer Reviewed: 6 results) Presentation (3 results)

  • [Journal Article] Comparison of the catalytic activities of three isozymes of carnitine palmitoyltransferase 1 expressed in COS7 cells2014

    • Author(s)
      Hada T, Yamamoto T, Yamamoto A, Ohkura K, Yamazaki N, Takiguchi Y, Shinohara Y
    • Journal Title

      Appl Biochem Biotechnol

      Volume: 172 Pages: 1486-1496

    • Peer Reviewed
  • [Journal Article] Molecular basis of interactions between mitochondrial proteins and hydroxyapatite in the presence of Triton X-100, as revealed by proteomic and recombinant techniques2013

    • Author(s)
      Yamamoto T, Tamaki H, Katsuda C, Nakatani K, Terauchi S, Terada H, Shinohara Y
    • Journal Title

      J Chromatogr A

      Volume: 1301 Pages: 169-178

    • Peer Reviewed
  • [Journal Article] Pseudogenes of rat VDAC1 : 16 gene segments in the rat genome show structural similarities with the cDNA encoding rat VDAC1, with 8 slightly expressed in certain tissues2012

    • Author(s)
      Ido Y, Yamamoto T, Yoshitomi T, Yamamoto A, Obana E, Ohkura K, Shinohara Y
    • Journal Title

      Mamm Genome

      Volume: 23 Pages: 286-293

    • Peer Reviewed
  • [Journal Article] Comparison of two expression systems using COS7 cells and yeast cells for expression of heart/muscle-type carnitine palmitoyltransferase 12012

    • Author(s)
      Hada T, Kato Y, Obana E, Yamamoto A, Yamazaki N, Hashimoto M, Yamamoto T, Shinohara Y
    • Journal Title

      Protein Expr Purif

      Volume: 82 Pages: 192-196

    • Peer Reviewed
  • [Journal Article] プロテオミクスで解き明かすミトコンドリアからのシトクロムc放出機構2012

    • Author(s)
      山本武範、山田安希子、吉村勇哉、寺田弘、篠原康雄
    • Journal Title

      薬学雑誌

      Volume: 132 Pages: 1099-1104

    • Peer Reviewed
  • [Journal Article] ヘキソキナーゼとがんの代謝2012

    • Author(s)
      尾華絵里子、安倍正博、山本武範、篠原康雄
    • Journal Title

      実験医学

      Volume: 30 Pages: 2370-2375

    • Peer Reviewed
  • [Presentation] 透過性遷移を誘起したミトコンドリアからのApoptosis-inducing factor(AIF)の漏出機構2013

    • Author(s)
      山本武範、吉村勇哉、山本篤司、山田安希子、寺田弘、篠原康雄
    • Organizer
      第35回生体膜と薬物の相互作用シンポジウム
    • Place of Presentation
      東京大学薬学部(東京都本郷)
    • Year and Date
      20131121-22
  • [Presentation] ミトコンドリアからのapoptosis-inducing factor(AIF)の漏出を促進する因子の同定と漏出したAIFの分子構造解析2013

    • Author(s)
      山本武範、吉村勇哉、山本篤司、懸山啓太、山田安希子、寺田弘、原島秀吉、篠原康雄
    • Organizer
      日本薬学会第133年会
    • Place of Presentation
      横浜パシフィコ(神奈川県横浜)
    • Year and Date
      20130327-30
  • [Presentation] 抗原抗体反応とプロテオミクスを用いたミトコンドリア外膜に存在するVDACアイソフォームの発現プロファイル解析2012

    • Author(s)
      山本武範、井戸佑介、中野裕美子、河野麻由、寺田弘、原島秀吉、篠原康雄
    • Organizer
      第27回日本DDS学会
    • Place of Presentation
      札幌コンベンションセンター(北海道札幌)
    • Year and Date
      2012-07-03

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Published: 2015-06-25  

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