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Development of the cell morphology database for drug and bioprobe discovery

Research Project

Project/Area Number 22710228
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Living organism molecular science
Research InstitutionThe Institute of Physical and Chemical Research

Principal Investigator

FUTAMURA Yushi  独立行政法人理化学研究所, 化学情報・化合物創製チーム, 特別研究員 (70525857)

Project Period (FY) 2010 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2010: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords細胞形態変化 / ハイコンテントスクリーニング / ケミカルバイオロジー / モルフォローム / 微生物代謝産物
Research Abstract

To discover small drug like molecules, we have constructed the encyclopedia of cellular morphology, consisting of the cell-shape changes induced by various compounds. Particularly, we have developed high-content image analysis method to examine the effect of~ 100 routinely used chemicals on the cell morphology accompanied by statistical characterization of the obtained phenotypic data. We demonstrated the cell morphology-based profiling system not only reproduces "drug-target-phenotype" relationships for a series of drugs with known targets but also raises the possibility to clear the way to discovery of unique drug candidates.

Report

(3 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • 2010 Annual Research Report
  • Research Products

    (7 results)

All 2011 2010

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (6 results)

  • [Journal Article] Vipirinin, a coumarin-based HIV-1 Vpr inhibitor, interacts with a hydrophobic region of VPR2011

    • Author(s)
      Futamura Y
    • Journal Title

      J. Biol. Chem

      Volume: 286 Pages: 14049-56

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Presentation] Identification of NPD3483 as a unique cell division inhibitor via the cell morphology-based screen2010

    • Author(s)
      Yushi Futamura, et al
    • Organizer
      22^<nd> EROTC-NCI-AACR symposium on Molecular Targets and Cancer Therapeutics
    • Place of Presentation
      Berlin, Germany
    • Year and Date
      2010-11-18
    • Related Report
      2010 Annual Research Report
  • [Presentation] The cell morphology-based screen revealed NPD3483 to be a unique type of cell division inhibitor2010

    • Author(s)
      二村友史, 他
    • Organizer
      第69回日本癌学会学術集会
    • Place of Presentation
      大阪
    • Year and Date
      2010-09-22
    • Related Report
      2010 Annual Research Report
  • [Presentation] Identification of NPD3483 as a unique cell division inhibitor via the cell morphology-based screen2010

    • Author(s)
      Futamura Y., Osada H.
    • Organizer
      22nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics
    • Place of Presentation
      ベルリン
    • Related Report
      2011 Final Research Report
  • [Presentation] Screening of bioactive compounds through morphology-based screens2010

    • Author(s)
      Futamura Y., Osada H.
    • Organizer
      Chemical Biology International Symposium
    • Place of Presentation
      埼玉
    • Related Report
      2011 Final Research Report
  • [Presentation] The cell morphology-based screen revealed NPD3483 to be a unique type of cell division inhibitor2010

    • Author(s)
      Futamura Y., Osada H.
    • Organizer
      69th Annual Meeting of the Japanese Cancer Association
    • Place of Presentation
      大阪
    • Related Report
      2011 Final Research Report
  • [Presentation] 細胞形態変化を指標としたがん分子標的治療薬の探索研究2010

    • Author(s)
      二村友史、長田裕
    • Organizer
      第14回日本がん分子標的治療学会学術集会
    • Place of Presentation
      東京
    • Related Report
      2011 Final Research Report 2010 Annual Research Report

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Published: 2010-08-23   Modified: 2016-04-21  

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