| Literature DB >> 27812771 |
Rana El Masri1,2,3, Amal Seffouh1,2,3, Hugues Lortat-Jacob1,2,3, Romain R Vivès4,5,6.
Abstract
The biological properties of Heparan sulfate (HS) polysaccharides essentially rely on their ability to bind and modulate a multitude of protein ligands. These interactions involve internal oligosaccharide sequences defined by their sulfation patterns. Amongst these, the 6-O-sulfation of HS contributes significantly to the polysaccharide structural diversity and is critically involved in the binding of many proteins. HS 6-O-sulfation is catalyzed by 6-O-sulfotransferases (6OSTs) during biosynthesis, and it is further modified by the post-synthetic action of 6-O-endosulfatases (Sulfs), two enzyme families that remain poorly characterized. The aim of the present review is to summarize the contribution of 6-O-sulfates in HS structure/function relationships and to discuss the present knowledge on the complex mechanisms regulating HS 6-O-sulfation.Entities:
Keywords: Biosynthesis; Glycosaminoglycan; Interaction; Structure/function relationships; Sulfatase
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Year: 2016 PMID: 27812771 DOI: 10.1007/s10719-016-9736-5
Source DB: PubMed Journal: Glycoconj J ISSN: 0282-0080 Impact factor: 2.916