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Profiling of N-glycan structure on GLUT4 glucose transporter critical for intracellular trafficking

Research Project

Project/Area Number 15K18509
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Functional biochemistry
Research InstitutionJapanese Foundation for Cancer Research

Principal Investigator

HAGA Yoshimi  公益財団法人がん研究会, ゲノムセンター, 研究員 (40525789)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2016: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords糖鎖 / 質量分析 / GLUT4
Outline of Final Research Achievements

The facilitative glucose transporter GLUT4 plays a key role in regulating whole-body glucose homeostasis. To elucidate the functional significance of the sole N-glycan chain on GLUT4, wild-type GLUT4 and a GLUT4-glycosylation mutant conjugated with EGFP were stably expressed in HeLa cells and its N-glycoforms were analyzed by mass spectrometer. Kifunensine-treated cells lost sensitivity to insulin, suggesting the functional importance of the N-glycan structure for GLUT4 trafficking. Large, unique structures were detected on insulin-responsive GLUT4, suggesting that a specific structural element of N-glycan may be critical for the localization of GLUT4 to the appropriate intracellular pool essential for insulin-mediated translocation, and part of the N-glycan structure has the potential to act as a sorting signal.

Report

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

    (4 results)

All 2016 2015

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (3 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Morphological Changes, Cadherin Switching, and Growth Suppression in Pancreatic Cancer by GALNT6 Knockdown2016

    • Author(s)
      Tarhan, Y. E., Kato, T., Jang, M., Haga, Y., Ueda, K., Nakamura, Y. and Park, J. H.
    • Journal Title

      Neoplasia

      Volume: 18 Issue: 5 Pages: 265-72

    • DOI

      10.1016/j.neo.2016.03.005

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Development of rapid glycoform analysis for specificity-enhanced PSA screening2016

    • Author(s)
      Yoshimi Haga, Motohide Uemura and Koji Ueda
    • Organizer
      第75回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2016-10-08
    • Related Report
      2016 Annual Research Report
  • [Presentation] Development of specificity-enhanced PSA screening by rapid glycoform analysis2016

    • Author(s)
      Yoshimi Haga, Naomi Saichi, Motohide Uemura and Koji Ueda
    • Organizer
      Tenth AACR-JCA Joint Conference on Breakthroughs in Cancer Research
    • Place of Presentation
      マウイ島、アメリカ
    • Year and Date
      2016-02-19
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] Development of specificity-enhanced PSA by rapid glycan profiling2015

    • Author(s)
      Yoshimi Haga, Naomi Saichi and Koji Ueda
    • Organizer
      HUPO 2015
    • Place of Presentation
      バンクーバー、カナダ
    • Year and Date
      2015-09-28
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research

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

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