Mapping and quantification of the major oligosaccharide components of heparin
Autor: | Duraikkannu Loganathan, Robert J. Linhardt, D L Lohse, Hui M. Wang, Yeong Shik Kim, Kevin G. Rice |
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Rok vydání: | 1988 |
Předmět: |
Swine
Antithrombin III Oligosaccharides Biochemistry Glycosaminoglycan chemistry.chemical_compound Affinity chromatography Methods medicine Animals Chondroitin Binding site Molecular Biology Chromatography High Pressure Liquid chemistry.chemical_classification Binding Sites Chromatography Heparin Antithrombin Cell Biology Oligosaccharide Heparin lyase chemistry Cattle Research Article medicine.drug |
Zdroj: | Biochemical Journal. 254:781-787 |
ISSN: | 1470-8728 0264-6021 |
DOI: | 10.1042/bj2540781 |
Popis: | A new method of determining the oligosaccharide composition of commercial glycosaminoglycan heparin is described in which heparin was first depolymerized using heparin lyase (EC 4.2.2.7), and then analysed by a single h.p.l.c. step. All 20 of the porcine and bovine heparins examined were found to contain a small number of major oligosaccharide components, which on average comprised 86% of their mass. The five most abundant oligosaccharides have defined chemical structures. Although the relative abundance of oligosaccharides varied, the heparins examined were surprisingly similar. Porcine, bovine, low-Mr, and high and low antithrombin III (ATIII)-affinity heparins, however, each had distinctly different proportions of these major oligosaccharide components. The concentrations of one of these five oligosaccharides, containing a portion of the ATIII binding site, correlated with the anticoagulant activity of the ATIII-affinity-fractionated porcine-mucosal heparins from which it was derived. An additional oligosaccharide of undetermined structure was found in significant quantities in both bovine heparin and high ATIII-affinity porcine-mucosal heparin. The correlation between oligosaccharide concentration and anticoagulant activity suggests that the oligosaccharide is derived from a structural variant of the ATIII-binding site. Finally, for the heparins examined chondroitin/dermatan sulphate formed 0.6-7.4% of their mass. |
Databáze: | OpenAIRE |
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