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Development of a comprehensive drug transporter identification method by gene knockout

Research Project

Project/Area Number 15K14998
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Medical pharmacy
Research InstitutionThe University of Tokyo

Principal Investigator

Kusuhara Hiroyuki  東京大学, 大学院薬学系研究科(薬学部), 教授 (00302612)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsトランスポーター / CRISPR-Cas9システム / 発現抑制 / オーファントランスポーター / CRISPR-Cas9 / 遺伝子ノックアウト / ほ乳類細胞 / CRISPR Cas9システム / ライブラリー / レンチウィルス
Outline of Final Research Achievements

The aim of this research was to establish inhibition of transporter gene expression by CRISPR-Cas9 system in mammalian cells as transporter identification tool. We designed guide RNA for all human SLC transporters and succeeded in simultaneous knockout of multiple transporters. On the other hand, we failed to suppress expression of some genes in the host cells after infection of viruses. Improvements in the design method of guide RNA are future subjects.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • Research Products

    (1 results)

All 2016

All Presentation (1 results)

  • [Presentation] Investigation of substrate specificity of mouse and human SLC35F2 in HEK293 cells2016

    • Author(s)
      Mochizuki T, Mizuno T, Kusuhara H
    • Organizer
      日本薬物動態学会 第31回年会
    • Place of Presentation
      キッセイ文化ホール(長野県松本市)
    • Year and Date
      2016-10-13
    • Related Report
      2016 Annual Research Report

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Published: 2015-04-16   Modified: 2018-03-22  

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