Literature DB >> 1859357

Sequence analysis of heparan sulphate indicates defined location of N-sulphated glucosamine and iduronate 2-sulphate residues proximal to the protein-linkage region.

J E Turnbull1, J T Gallagher.   

Abstract

A strategy that we originally used to identify an N-acetylated domain adjacent to the protein-linkage sequence of heparan sulphate proteoglycan (HSPG) [Lyon, Steward, Hampson & Gallagher (1987) Biochem. J. 242, 493-498] has been adapted for analysis of the location of GlcNSO3-HexA and GlcNSO3(+/- 6S)-IdoA(2S) units most proximal to the core protein. [3H]Glucosamine-labelled HSPG from human skin fibroblasts was depolymerized by using HNO2 or heparinase under conditions that allowed cleavage of all susceptible linkages. The degraded PG was coupled to Sepharose beads through the protein component, enabling specific recovery of protein-linked resistant oligosaccharides. These were released by treatment with alkaline borohydride and analysed by gel filtration and gradient PAGE. This strategy allowed investigation of the sequence of sugar residues along the chain relative to a common reference point (i.e. the reducing end of the chain). HNO2 scission confirmed the presence of a well-defined N-acetylated sequence predominantly 9-12 disaccharide units in length proximal to the core protein. Heparinase scission produced two classes of oligosaccharides (Mr approx. 7000 and 15,000) with the general formula: IdoA(2S)-GlcNSO3-[HexA-GlcNR]n-HexA-GlcNSO3-[Hex A-GlcNAc]9 12-GlcA-Gal-Gal-Xyl in which the average value for n is 1-2 for the 7000-Mr species and approx. 22 for the 15,000-Mr species. The latter oligosaccharides extend to about one-third of the total length of the HS chains (Mr approx. 45,000). HNO2 scission of these oligosaccharides enabled hypothetical models for their sequence to be proposed. The general arrangement of N-sulphated and N-acetylated disaccharides between the proximal GlcNSO3 and terminal IdoA(2S) residues of the 15,000-Mr fragment was similar to that in the original polysaccharide, suggesting the possibility of a tandemly repeating pattern in the sequence of HS.

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Year:  1991        PMID: 1859357      PMCID: PMC1151232          DOI: 10.1042/bj2770297

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  30 in total

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Authors:  L G Oscarsson; G Pejler; U Lindahl
Journal:  J Biol Chem       Date:  1989-01-05       Impact factor: 5.157

2.  Biosynthesis of heparin. Relationship between the polymerization and sulphation processes.

Authors:  K Lidholt; L Kjellén; U Lindahl
Journal:  Biochem J       Date:  1989-08-01       Impact factor: 3.857

3.  Oligosaccharide mapping of heparan sulphate by polyacrylamide-gradient-gel electrophoresis and electrotransfer to nylon membrane.

Authors:  J E Turnbull; J T Gallagher
Journal:  Biochem J       Date:  1988-04-15       Impact factor: 3.857

4.  Constant and variable domains of different disaccharide structure in corneal keratan sulphate chains.

Authors:  M Oeben; R Keller; H W Stuhlsatz; H Greiling
Journal:  Biochem J       Date:  1987-11-15       Impact factor: 3.857

Review 5.  Structure and function of heparan sulphate proteoglycans.

Authors:  J T Gallagher; M Lyon; W P Steward
Journal:  Biochem J       Date:  1986-06-01       Impact factor: 3.857

6.  Analysis of heparan sulfate from the Engelbreth-Holm-Swarm (EHS) tumor.

Authors:  P V Trescony; T R Oegema; B J Farnam; L B Deloria
Journal:  Connect Tissue Res       Date:  1989       Impact factor: 3.417

7.  Molecular distinctions between heparan sulphate and heparin. Analysis of sulphation patterns indicates that heparan sulphate and heparin are separate families of N-sulphated polysaccharides.

Authors:  J T Gallagher; A Walker
Journal:  Biochem J       Date:  1985-09-15       Impact factor: 3.857

8.  Structure of the heparan sulfate-protein linkage region. Demonstration of the sequence galactosyl-galactosyl-xylose-2-phosphate.

Authors:  L A Fransson; I Silverberg; I Carlstedt
Journal:  J Biol Chem       Date:  1985-11-25       Impact factor: 5.157

9.  Evidence of random structural features in the heparin polymer.

Authors:  R J Linhardt; Z M Merchant; K G Rice; Y S Kim; G L Fitzgerald; A C Grant; R Langer
Journal:  Biochemistry       Date:  1985-12-17       Impact factor: 3.162

10.  Heparin sequences in the heparan sulfate chains of an endothelial cell proteoglycan.

Authors:  H B Nader; C P Dietrich; V Buonassisi; P Colburn
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

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3.  Binding and clustering of glycosaminoglycans: a common property of mono- and multivalent cell-penetrating compounds.

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Journal:  Biophys J       Date:  2007-12-07       Impact factor: 4.033

4.  Binding of endostatin to endothelial heparan sulphate shows a differential requirement for specific sulphates.

Authors:  Fiona H Blackhall; Catherine L R Merry; Malcolm Lyon; Gordon C Jayson; Judah Folkman; Kashi Javaherian; John T Gallagher
Journal:  Biochem J       Date:  2003-10-01       Impact factor: 3.857

5.  The proteoglycan bikunin has a defined sequence.

Authors:  Mellisa Ly; Franklin E Leach; Tatiana N Laremore; Toshihiko Toida; I Jonathan Amster; Robert J Linhardt
Journal:  Nat Chem Biol       Date:  2011-10-09       Impact factor: 15.040

6.  Glycomics approaches for the bioassay and structural analysis of heparin/heparan sulphates.

Authors:  Tania M Puvirajesinghe; Jeremy E Turnbull
Journal:  Metabolites       Date:  2012-11-28

7.  An integrated approach using orthogonal analytical techniques to characterize heparan sulfate structure.

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  7 in total

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