Literature DB >> 2530916

A simple procedure for the preparation and purification of the oligosaccharide components of the glycosylphosphatidylinositol anchor of membrane proteins.

A S Kennington1, T Y Shen, G Romero.   

Abstract

The oligosaccharide components of the glycosylphosphatidylinositol anchors of Trypanosoma brucei variant surface glycoproteins have been prepared and purified by treatment with hydrolytic enzymes and solvent extraction procedures followed by HPLC purification using a specific oligosaccharide binding matrix (Glyco-Pak N, by Waters). Three oligosaccharide peaks (peaks I, II and III) were resolved by a single isocratic HPLC step (70% acetonitrile in water). The material from these peaks was hydrolyzed in acid and analyzed by GC/MS. GC/MS analysis of the material obtained from each peak demonstrated the presence of inositol, glucosamine, and mannose in a 1:1:3 ratio. A variable number of galactose residues were detected in each peak. The galactose:inositol ratios of the purified components were 1:1, 2:1, and 3:1 for peaks I, II and III, respectively, suggesting that the separation obtained depends primarily on the number of sugar residues present in each fraction.

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Year:  1989        PMID: 2530916     DOI: 10.1016/0003-2697(89)90384-9

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  1 in total

1.  Anti-inositolglycan antibodies selectively block some of the actions of insulin in intact BC3H1 cells.

Authors:  G Romero; G Gámez; L C Huang; K Lilley; L Luttrell
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

  1 in total

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