Chemical modification of heparin and heparosan

Methods Mol Biol. 2015:1229:31-6. doi: 10.1007/978-1-4939-1714-3_4.

Abstract

Heparin is a potent clinically used anticoagulant. It is a heterogeneous mixture of polymers that contain a variety of sulfation patterns. However, only 3-O sulfonated heparin pentasaccharide units have been proven to bind to antithrombin and elicit an anticoagulant response. Heparins with other sulfation patterns are able to bind to a variety of other proteins such as FGF, VEGF, and CXCL-3. By modulating heparin's sulfation pattern, it is possible to generate polymers that can regulate biological processes beyond hemostasis. Here we describe a variety of simple chemical modification methods, N-acetylation, N-deacetylation, N-sulfation, O-sulfation, 2-O desulfation, and complete desulfation, to prepare heparin-like polymers with distinct sulfation patterns.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetylation
  • Biochemistry / methods*
  • Disaccharides / chemistry*
  • Heparin / chemistry*
  • Polymers / chemistry
  • Pyridinium Compounds / chemistry
  • Quaternary Ammonium Compounds / chemistry
  • Salts / chemistry
  • Sulfates / chemistry

Substances

  • Disaccharides
  • Polymers
  • Pyridinium Compounds
  • Quaternary Ammonium Compounds
  • Salts
  • Sulfates
  • heparosan
  • tri-n-butylmethylammonium
  • Heparin