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High time resolution FRET analysis of the activation of G protein

Research Project

Project/Area Number 23590270
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field General physiology
Research InstitutionNational Institute for Physiological Sciences

Principal Investigator

TATEYAMA Michihiro  生理学研究所, 分子生理研究系, 准教授 (30276472)

Co-Investigator(Renkei-kenkyūsha) KUBO Yoshihiro  生理学研究所, 分子生理研究系, 教授 (80211887)
Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2013: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2012: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2011: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
KeywordsGタンパク質共役型受容体 / FRET / Gタンパク質 / GPCR / G protein / imaging / kinetics / receptor
Research Abstract

G protein coupled receptors (GPCRs) are the important signaling molecules which are activated upon the binding with the specific ligand and trigger the downstream signaling through activating G protein. These initial processes of GPCR signaling, the activation of receptor and the following G protein binding, were analyzed by using a fluorescence resonance energy transfer (FRET) technique. With the high time resolution FRET analysis, we found that binding of G protein stabilizes the active conformations of GPCRs and slows the deactivation of the activated receptor. Further FRET studies revealed that the effects of G protein binding differ depending on the type of the coupled receptors.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (14 results)

All 2013 2012 2011 Other

All Journal Article (5 results) (of which Peer Reviewed: 3 results) Presentation (9 results)

  • [Journal Article] Analyses of the effects of Gq protein on the activated states of the muscarinic M3 receptor and the purinergic P2Y1 receptor2013

    • Author(s)
      Tateyama M and Kubo Y
    • Journal Title

      Physiological Reports

      Volume: 1(5) Issue: 5

    • DOI

      10.1002/phy2.134

    • Related Report
      2013 Annual Research Report 2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] Binding of Gq protein stabilizes the activated state of the muscarinic receptor type 12013

    • Author(s)
      Tateyama, M., Kubo, Y
    • Journal Title

      Neuropharmacol.

      Volume: 65 Pages: 173-183

    • DOI

      10.1016/j.neuropharm.2012.10.006

    • Related Report
      2013 Annual Research Report 2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] GABA_B受容体の構造と機能2012

    • Author(s)
      立山充博, 松下真一, 久保義弘
    • Journal Title

      臨床神経科学(中外医学社)

      Volume: 30巻第12号 Pages: 1349-1351

    • Related Report
      2013 Final Research Report
  • [Journal Article] GABAB受容体の構造と機能2012

    • Author(s)
      立山充博、松下真一、久保義弘
    • Journal Title

      臨床神経科学

      Volume: 30 Pages: 1349-1351

    • Related Report
      2012 Research-status Report
  • [Journal Article] The intra-molecular activation mechanisms of the dimeric metabotropic glutamate receptor 1 differ depending on the type of G proteins2011

    • Author(s)
      Tateyama, M., Kubo, Y
    • Journal Title

      Neuropharmacol.

      Volume: 61 Issue: 4 Pages: 832-841

    • DOI

      10.1016/j.neuropharm.2011.05.031

    • Related Report
      2013 Final Research Report 2011 Research-status Report
    • Peer Reviewed
  • [Presentation] FRET analysis of G protein coupled receptors2012

    • Author(s)
      立山充博, 松下真一, 久保義弘
    • Organizer
      シンポジウム「イメージングより明らかにされたGタンパク質共役型受容体のダイナミクス」第134回日本薬学会年会
    • Place of Presentation
      札幌
    • Year and Date
      2012-03-30
    • Related Report
      2013 Final Research Report
  • [Presentation] FRETによる受容体活性化過程の可視化2012

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第132回日本薬学会(招待講演)
    • Place of Presentation
      北海道大学・高等教育推進機構(北海道)
    • Related Report
      2011 Research-status Report
  • [Presentation] The intra-molecular activation mechanisms of the dimeric metabo- tropic glutamate receptor1 differ depending on the type of the coupled G-protein2011

    • Author(s)
      立山充博, 久保義弘
    • Organizer
      シンポジウム「GPCRシグナル伝達の構造と機能:創薬への新たな展開」第84回日本生化学大会
    • Place of Presentation
      京都
    • Year and Date
      2011-09-22
    • Related Report
      2013 Final Research Report
  • [Presentation] m1ムスカリン受容体とGqタンパク質会合のFRET解析2011

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第34回日本神経科学大会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Related Report
      2011 Research-status Report
  • [Presentation] ホモ2量体代謝型グルタミン酸受容体1型の分子内活性化機構は、結合するGタンパク質の種類によって異なる2011

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第84回日本生化学会大会(招待講演)
    • Place of Presentation
      国立京都国際会館(京都府)
    • Related Report
      2011 Research-status Report
  • [Presentation] FRET analyses of the stabilizing effect of Gi1 protein on the agonist-induced activated conformation of the A1aR

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第36回日本神経科学大会
    • Place of Presentation
      国際会議場(京都府)
    • Related Report
      2013 Annual Research Report
  • [Presentation] Stabilizing effects of G protein on the active conformation of the adenosine receptor type 1a differ depending on the type of G protein

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第91回日本生理学会大会
    • Place of Presentation
      鹿児島大学郡元キャンパス(鹿児島県)
    • Related Report
      2013 Annual Research Report
  • [Presentation] 受容体活性化状態に対するGqタンパク質の作用は受容体ごとに

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第35回日本神経科学大会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Related Report
      2012 Research-status Report
  • [Presentation] Gqタンパク質はM1RおよびM3Rの活性型構造に対し安定化作用を示すがP2Y1Rでは安定化作用を示さない

    • Author(s)
      立山充博、久保義弘
    • Organizer
      第90回日本生理学会大会
    • Place of Presentation
      タワーホール船堀(東京都)
    • Related Report
      2012 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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