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Analysis of sperm proteins involved in mammalian fertilization

Research Project

Project/Area Number 17590240
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General medical chemistry
Research InstitutionThe University of Tokyo

Principal Investigator

TAKASAKI Seiichi  The University of Tokyo, Institute of Medical Science, Associate Professor, 医科学研究所, 助教授 (80112093)

Project Period (FY) 2005 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2006: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2005: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsfertilization / sperm / carbohydrate recognition molecule / 接着活性
Research Abstract

A multiple carbohydrate recognition mechanism is working in fertilization. We have shown that several moleculesrecognizing egg zona pellucida glycoproteins are expressed on boar sperm heads.
In this project, carbohydrate recognition molecules on boar sperm were investigated. When detergent-solubilized plasma membranes of boar sperm were applied to plastic wells coated with the N-acetyllactoamine-oligosaccharide probe, two molecules(70 kDa and 40 kDa) bound to the wells and binding was inhibited by addition of the oligosaccharides. Both molecules were also shown to have affinity to asialo-alpha-1-acid glycoprotein which contains N-acetyllactosamine-oligosacharides. Partial amino acid sequences of tryptic peptide fragments of the two proteins were determined. Homology search of the peptide sequences suggested that the 70 and 40 kDa molecules are members of ADAM(a disintegrin and metalloprotease protein)family protein. cDNA encoding the proteins were cloned and their nucleotide sequences were determined. Then, the recombinant proteins of porcine ADAM4 were produced by yeast and the purified proteins were shown to have affinity to integrins. The recombinant proteins of porcine ADAM5 expressed on the surface of mammalian cells were also shown to bind to asialo-fetun but not to agalacto-fetuin, suggesting that ADAM5 is a carbohydrate recognition molecule recognizing the N-acetyllactosamine structure.

Report

(3 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report
  • Research Products

    (3 results)

All 2006

All Journal Article (3 results)

  • [Journal Article] The analysis of N-glycolylneuraminic acid)NeuGc) of hepatoma tissue and K562 cell ferritins using HPLC and mass spectrometry2006

    • Author(s)
      Asakawa, H
    • Journal Title

      Proc. Jpn. Acad., Ser.B 82

      Pages: 181-187

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] The analysis of N-glycolylneuraminic acid(NeuGc) of hepatoma tissue and K562 cell ferritins using HPLC and mass spectrometry2006

    • Author(s)
      Asakawa, H.
    • Journal Title

      Proc.Jpn.Acad., Ser.B. 80

      Pages: 181-187

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] The analysis of N-glycolylneuraminic acid (NeuGc) of hepatoma tissue and K562 cell ferritins using HPLC and mass spectrometry2006

    • Author(s)
      Asakawa, H.
    • Journal Title

      Proc. Jpn. Acad., Ser. B 82

      Pages: 181-187

    • Related Report
      2006 Annual Research Report

URL: 

Published: 2005-04-01   Modified: 2016-04-21  

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