• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Studies on Molecular Recognition Patterns between Sugars and Amino Acids by Use of the Data Obtained from Single Crystal X-Ray Analysis

Research Project

Project/Area Number 04453158
Research Category

Grant-in-Aid for General Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field 結晶学
Research InstitutionTokai University

Principal Investigator

HIRAYAMA Noriaki  Tokai University, Department of Biological Science & Technology, professor, 開発工学部, 教授 (70238393)

Co-Investigator(Kenkyū-buntansha) FUJII Isao  Tokai University, Department of Biological Science & Technology, research assist, 開発工学部, 助手 (60238524)
SUDA Hitosh  Tokai University, Department of Biological Science & Technology, lecturer, 開発工学部, 講師 (70216472)
Project Period (FY) 1992 – 1994
Project Status Completed (Fiscal Year 1994)
Budget Amount *help
¥8,000,000 (Direct Cost: ¥8,000,000)
Fiscal Year 1994: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1993: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1992: ¥5,700,000 (Direct Cost: ¥5,700,000)
Keywordssugar-amino acid interactions / molecular mechanics / single crystal X-ray analysis / molecular recognition / crystallization / 糖ーアミノ酸相互作用 / 自動結晶化法
Research Abstract

Structural investigations of oligosaccharides and studies on recognition patterns between sugars and proteins are very essential to the understanding of biological functions sugars. In the present study we have undertaken the conformational analysis of one of the most biologically important oligosaccharides, sialyl Le^X, and the analysis of the interaction patterns between sugars and amino acids in protein structures which have been determined by X-ray analysis.
1.Conformational analysis of sialy Le^X by molecular mechanics
Since suitable crystals of the sugar chain for diffraction experiments could not be obtained, the conformation of the sugar chain was investigated by molecular mechanics calculations. The initial models were constructed by docking X-ray structures of the component monosaccharides through glycosidic bonds and they were optimized by molecular mechanics. Two different docking modes were applied.It was shown that the docking mode influence the resultant stable conformations signficantly.
2.Analysis of interaction patterns between sugars and amino acids in proteins
Interaction patterns between selected monosaccharides and amino acids in the proteins have been investigated by use of the X-ray data. All the X-ray data were taken from Protein Databank compiled at Brookhaven National Laboratory (USA). The monosaccharides which were taken into consideration are N-acetyl-glucosamine, arabinose, fucose, galactose, glucose, mannose, sialic acid, and zylose. Hydrogen bonds, non-bonded interactions, and interactions between sugars and aromatic rings were taken into account. The analysis showed that there is a specific common binding pocket for sugars in proteins. The pocket is consist of two layrs of amino acids. The inner layr in which amino acids participate in hydrogen bonds is made of mainly hydrophilic amino acids. The outer layr is chiefly consist of hydrophobic amino acids.

Report

(4 results)
  • 1994 Annual Research Report   Final Research Report Summary
  • 1993 Annual Research Report
  • 1992 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] N.Hirayama,N.Yoda,and T.Nishi: "Conformation Analysis of Sialy Le^X by Molecular Mechanics" Chemistry Letters. 1994. 1479-1482 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] N.Hirayama, N.Yoda and T.Nishi: "Conformation Analysis of Sialyl Le^X by Molecular Mdchanics" Chemistry Letters. 1994. 1479-1482 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1994 Final Research Report Summary
  • [Publications] N.Hirayama,N.Yoda and T.Nishi: "Conformation Analysis of Sialyl Lex by Molecular Mechanics" Chemistry Letters. 1994. 1479-1482 (1994)

    • Related Report
      1994 Annual Research Report

URL: 

Published: 1992-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi