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dc.contributor.authorMurphy, Kevin J
dc.contributor.authorMerry, Catherine L R
dc.contributor.authorLyon, Malcolm
dc.contributor.authorThompson, James E
dc.contributor.authorRoberts, Ian S
dc.contributor.authorGallagher, John T
dc.date.accessioned2009-08-25T11:25:49Z
dc.date.available2009-08-25T11:25:49Z
dc.date.issued2004-06-25
dc.identifier.citationA new model for the domain structure of heparan sulfate based on the novel specificity of K5 lyase. 2004, 279 (26):27239-45 J. Biol. Chem.en
dc.identifier.issn0021-9258
dc.identifier.pmid15047699
dc.identifier.doi10.1074/jbc.M401774200
dc.identifier.urihttp://hdl.handle.net/10541/78452
dc.description.abstractElucidation of the molecular structure of heparan sulfate (HS) is the key to understanding its functional versatility as a co-receptor for growth factors and morphogens. We have identified and exploited the novel substrate specificity of the coliphage K5 lyase in studies of the domain organization of HS. We show that K5 lyase cleaves HS principally within non-sulfated sequences of four or more N-acetylated disaccharides. Uniquely, sections comprising alternating N-acetylated and N-sulfated units are resistant to the enzyme, as are the highly sulfated S domains. Spacing of the K5 lyase cleavage sites ( approximately 7-8 kDa) is similar to that of the S domains. On the basis of these findings, we propose a refined model of the structure of HS in which N-acetylated sequences of four to five disaccharide units (GlcNAc-GlcUA)(4-5) are positioned centrally between the S domains. The latter are embedded within N-acetylated and N-sulfated sequences, forming extended regions of hypervariable sulfation distributed at regular intervals along the polymer chain. K5 lyase provides a means of excision of these composite sulfated regions for structural and functional analyses.
dc.language.isoenen
dc.subject.meshChromatography, Gel
dc.subject.meshDisaccharides
dc.subject.meshEscherichia coli Proteins
dc.subject.meshFlavobacterium
dc.subject.meshGlucosamine
dc.subject.meshHeparin Lyase
dc.subject.meshHeparitin Sulfate
dc.subject.meshModels, Molecular
dc.subject.meshNitrous Acid
dc.subject.meshOligosaccharides
dc.subject.meshPolysaccharide-Lyases
dc.subject.meshProtein Structure, Tertiary
dc.subject.meshRecombinant Proteins
dc.subject.meshSubstrate Specificity
dc.subject.meshTritium
dc.titleA new model for the domain structure of heparan sulfate based on the novel specificity of K5 lyase.en
dc.typeArticleen
dc.contributor.departmentCancer Research UK and University of Manchester, Department of Medical Oncology, Christie Hospital NHS Trust, Wilmslow Road, Manchester M20 4BX, United Kingdom.en
dc.identifier.journalThe Journal of Biological Chemistryen
html.description.abstractElucidation of the molecular structure of heparan sulfate (HS) is the key to understanding its functional versatility as a co-receptor for growth factors and morphogens. We have identified and exploited the novel substrate specificity of the coliphage K5 lyase in studies of the domain organization of HS. We show that K5 lyase cleaves HS principally within non-sulfated sequences of four or more N-acetylated disaccharides. Uniquely, sections comprising alternating N-acetylated and N-sulfated units are resistant to the enzyme, as are the highly sulfated S domains. Spacing of the K5 lyase cleavage sites ( approximately 7-8 kDa) is similar to that of the S domains. On the basis of these findings, we propose a refined model of the structure of HS in which N-acetylated sequences of four to five disaccharide units (GlcNAc-GlcUA)(4-5) are positioned centrally between the S domains. The latter are embedded within N-acetylated and N-sulfated sequences, forming extended regions of hypervariable sulfation distributed at regular intervals along the polymer chain. K5 lyase provides a means of excision of these composite sulfated regions for structural and functional analyses.


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