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in vivo biochemistry using optogenetics of cell signaling and FRET probe

Research Project

Project/Area Number 25670088
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field General anatomy (including histology/embryology)
Research InstitutionTokyo Medical and Dental University

Principal Investigator

NAKATA Takao  東京医科歯科大学, 医歯(薬)学総合研究科, 教授 (50218004)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords光スイッチ / 解剖学 / 細胞組織 / シグナル伝達 / 神経科学
Outline of Final Research Achievements

The difference between cellls and chemical reaction in test tube was probably each reaction was properly organized in time and space. However,how the chemical reactions propagate in cells were still unknown. Actin is one of the most fundammental protein for cell motility and cytoarchitecture. However, its study on their regulatory mechanisms were not progressed for this 25 years, such as CDC42 and RAC1 polymerize actin filamnes of filopodia and lamelli podia. We use photoswitch of CDC42 and RAC1to regulate spatiotemporal regulation of these proteins, and monitor the cellular phenotypes using the FRET sensor and Life-act m Cherry markers,

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (1 results)

All 2015

All Presentation (1 results)

  • [Presentation] 光遺伝学を用いた分泌経路の研究2015

    • Author(s)
      中田隆夫
    • Organizer
      第120 回日本解剖学会総会 全国学術集会
    • Place of Presentation
      神戸
    • Year and Date
      2015-03-21
    • Related Report
      2014 Annual Research Report

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Published: 2014-07-25   Modified: 2019-07-29  

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