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脂質と抗原提示タンパク質の相互作用の解明を目指した結合分子の合成と生物活性評価

Research Project

Project/Area Number 16J01933
Research Category

Grant-in-Aid for JSPS Fellows

Allocation TypeSingle-year Grants
Section国内
Research Field Biomolecular chemistry
Research InstitutionOsaka University

Principal Investigator

HOSSAIN MD. IMRAN  大阪大学, 理学研究科, 特別研究員(PD)

Project Period (FY) 2016-04-22 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2017: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2016: ¥700,000 (Direct Cost: ¥700,000)
Keywordsglycosphingolipid / glycosylation / interaction / immunity / GalCer, / Glycosylation / KRN7000 / CD1d / Cytokines / Natural productcs
Outline of Annual Research Achievements

We synthesized a novel series of lysophosphatidylethanolamine, which are derivatives of NKT activating plasmalogens (pLPE) isolated from mouse thymus. We have established SPR technique to examine the lipid-CD1d binding affinity and examined the binding affinity of the synthesized and some other intrinsic ligands with CD1d.
Human CD1d-β2M was immobilized on CM5 sensor chip and ligands solution was passed through the modified surface for the binding analysis. The kinetic measurement conditions are established first using standard ligand KRN7000, then the binding affinities of the synthesized and other natural lysophospholipids. All the lysophospholipids showed moderate dissociation constants (KD = 85 -253 nM) to the hCD1d immobilized surface. Cerotic acid used as a negative control, which showed no binding affinity with CD1d modified surface. Among the phospholipids, which have either double bond or p-fluoro benzyl group in the tail, showed slightly stronger binding affinities than the saturated or unsubstituted derivatives. The connectivity of head-tail groups does not show any significance in the binding affinity except vinyl-ether connection. Absence or presence of ethanolamine group showed significant difference in the binding affinity. On the other hand, ethanolamine to choline transformation did not show any binding activity difference.

Research Progress Status

29年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

29年度が最終年度であるため、記入しない。

Report

(2 results)
  • 2017 Annual Research Report
  • 2016 Annual Research Report
  • Research Products

    (4 results)

All 2016 Other

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Acknowledgement Compliant: 1 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] Synthesis and Th1-immunostimulatory activity of α-galactosylceramide analogues bearing a halogen-containing or selenium-containing acyl chain2016

    • Author(s)
      Md. Imran Hossain, Shinya Hanashima, Takuto Nomura, Sebastien Lethu, Hiroshi Tsuchikawa, Michio Murata, Hiroki Kusaka, Shunsuke Kita, Katsumi Maenaka
    • Journal Title

      Bioorganic & Medicinal Chemistry

      Volume: 24 Issue: 16 Pages: 3687-3695

    • DOI

      10.1016/j.bmc.2016.06.007

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Presentation] Synthesis and immunostimulatory activity of heavy atom labeled acyl chain containing α-GalCers2016

    • Author(s)
      Md. Imran Hossain
    • Organizer
      58th Symposium on Chemistry of Natural Products
    • Place of Presentation
      Sendai, Japan
    • Year and Date
      2016-09-14
    • Related Report
      2016 Annual Research Report
  • [Presentation] Synthesis and Immunostimulatory Activity of Heavy Atom Labeled Acyl Chain Containing α-GalCers for X-ray Crystal Analysis2016

    • Author(s)
      Md. Imran Hossain
    • Organizer
      2016 Natural Products and Bioactive Compounds Gordon Research Conference (GRC)
    • Place of Presentation
      Proctor Academy, Andover, NH, United States.
    • Year and Date
      2016-07-31
    • Related Report
      2016 Annual Research Report
  • [Remarks] Murata laboratory, Osaka university.

    • URL

      http://www.chem.sci.osaka-u.ac.jp/lab/murata/

    • Related Report
      2016 Annual Research Report

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Published: 2016-05-17   Modified: 2024-03-26  

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