Analysis of 3-O-sulfo group-containing heparin tetrasaccharides in heparin by liquid chromatography-mass spectrometry

Anal Biochem. 2014 Jun 15:455:3-9. doi: 10.1016/j.ab.2014.02.033. Epub 2014 Mar 28.

Abstract

Complete heparin digestion with heparin lyase 2 affords a mixture of disaccharides and resistant tetrasaccharides with 3-O-sulfo group-containing glucosamine residues at their reducing ends. Quantitative online liquid chromatography-mass spectrometric analysis of these resistant tetrasaccharides is described in this article. The disaccharide and tetrasaccharide compositions of seven porcine intestinal heparins and five low-molecular-weight heparins were analyzed by this method. These resistant tetrasaccharides account for from 5.3 to 7.3wt% of heparin and from 6.2 to 8.3wt% of low-molecular-weight heparin. Because these tetrasaccharides are derived from heparin's antithrombin III-binding sites, we examined whether this method could be applied to estimate the anticoagulant activity of heparin. The content of 3-O-sulfo group-containing tetrasaccharides in a heparin correlated positively (r=0.8294) to heparin's anticoagulant activity.

Keywords: 3-O-Sulfo group; Anticoagulant activity; Heparin lyase 2; Porcine intestinal heparin; RPIP–LC–MS; Tetrasaccharides.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticoagulants / chemistry
  • Anticoagulants / pharmacology
  • Antithrombin III / metabolism
  • Binding Sites
  • Carbohydrate Sequence
  • Chromatography, Liquid / methods*
  • Heparin Lyase / metabolism
  • Heparin, Low-Molecular-Weight / analysis*
  • Heparin, Low-Molecular-Weight / chemistry*
  • Heparin, Low-Molecular-Weight / metabolism
  • Heparin, Low-Molecular-Weight / pharmacology
  • Mass Spectrometry / methods*
  • Mass Spectrometry / standards
  • Molecular Sequence Data
  • Structure-Activity Relationship
  • Swine

Substances

  • Anticoagulants
  • Heparin, Low-Molecular-Weight
  • Antithrombin III
  • Heparin Lyase