Structural peculiarity and antithrombin binding region profile of mucosal bovine and porcine heparins

J Pharm Biomed Anal. 2016 Jan 25:118:52-63. doi: 10.1016/j.jpba.2015.10.001. Epub 2015 Oct 17.

Abstract

The major compositional differences between bovine mucosal heparin (BMH) and the currently employed porcine mucosal heparin (PMH) have been reported to essentially consist of reduced 6-O-sulfation of the glucosamine residues in BMH and somewhat lower 2-O-sulfation of the iduronate residues in PMH. The present work is based on direct comparison of several BMH and PMH commercial preparations. A combined study by 2D (heteronuclear single quantum coherence, HSQC) NMR and ion-pair reversed-phase high performance liquid chromatography (IPRP-HPLC) coupled with electrospray ionization mass spectrometry (ESI-MS) on the heparins, extended to the analysis of their heparinases digests and fractions separated by affinity chromatography on antithrombin (AT), confirmed the previously reported lower degree of 6-O-sulfation and showed lower 3-O-sulfated glucosamine content in BMH. More detailed studies allowed the identification of structural variants of AT-binding region (ATBR) structural variants, showing higher content of the N-sulfated components in BMH than in PMH.

Keywords: ATIII affinity chromatography; Bovine heparins; Liquid chromatography; Mass spectrometry; Nuclear magnetic resonance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antithrombins / chemistry*
  • Antithrombins / metabolism*
  • Binding Sites / physiology
  • Cattle
  • Chromatography, High Pressure Liquid / methods
  • Heparin / chemistry*
  • Heparin / metabolism*
  • Intestinal Mucosa / metabolism*
  • Magnetic Resonance Spectroscopy / methods
  • Swine

Substances

  • Antithrombins
  • Heparin