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Semin Thromb Hemost 2002; 28(4): 335-342
DOI: 10.1055/s-2002-34302
Copyright © 2002 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

Chemical Derivatization as a Strategy to Study Structure-Activity Relationships of Glycosaminoglycans

Benito Casu, Annamaria Naggi, Giangiacomo Torri
  • G. Ronzoni Institute for Chemical and Biochemical Research, Milan, Italy
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Publikationsverlauf

Publikationsdatum:
23. September 2002 (online)

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ABSTRACT

Sulfated glycosaminoglycans (GAGs) are amenable to a number of chemical modifications that modulate their biological activity. N-sulfate groups can be exposed and N-acylated (usually N-acetylated), specific O-sulfate groups can be removed, and free hydroxyl groups (either preexisting in the original GAG or exposed by desulfation) can be sulfated. Heparin/heparan sulfate, chondroitin sulfate, and dermatan sulfate have been variously desulfated or sulfated to afford novel GAGs with protein binding and associated biological properties different from those of the original GAGs. Regiospecific sulfation of N-acetyl heparosan (E. coli K5 polysaccharide) afforded a number of derivatives, some endowed with antithrombotic activity and others with antimetastatic properties. Most of the activities could be correlated with typical sulfation patterns along each GAG backbone. Glycol splitting of nonsulfated glucuronic residues (including a critical residue in the pentasaccharide sequence of the active site for antithrombin) leads to substantial loss of anticoagulant activity of heparin. Partial removal of sulfate groups at position 2 of iduronic acid residues followed by glycol splitting of all nonsulfated uronic acid residues afforded nonanticoagulant, antiangiogenic heparins.

KEYWORDS

Glycosaminoglycans - sulfation/desulfation - glycol splitting - structure-activity relationships

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