Extension and structural variability of the antithrombin-binding sequence in heparin

• Published in: The Journal of biological chemistry Vol. 259; no. 20; pp. 12368 - 12376
• Main Authors: Lindahl, U, Thunberg, L, Bäckström, G, Riesenfeld, J, Nordling, K, Björk, I
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 25.10.1984; American Society for Biochemistry and Molecular Biology
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Antithrombins; Biological and medical sciences; Borohydrides; Carbohydrate Sequence; Carbohydrates; Chemical Phenomena; Chemistry; Fundamental and applied biological sciences. Psychology; Heparin - isolation & purification; Intestinal Mucosa; Oligosaccharides - isolation & purification; Other biological molecules; Structure-Activity Relationship; Swine; Molecular structure; Oligosaccharide; Gut; Molecular interaction; Binding site; Antithrombin; Circular dichroism; Pig; Vertebrata; Mammalia; Affinity chromatography; Artiodactyla; Heparin; Spectrophotometry; Ungulata
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)90755-6

Oligosaccharides with different affinities for antithrombin were isolated following partial deaminative cleavage of pig mucosal heparin with nitrous acid. The smallest high-affinity component obtained was previously identified as an octasaccharide with the predominant structure: (Formula: see text). The interaction of this octasaccharide, and of deca- and dodecasaccharides containing the same octasaccharide sequence, with antithrombin was studied by spectroscopic techniques. The near-ultraviolet difference spectra, circular dichroism spectra, and fluorescence enhancements induced by adding these oligosaccharides to antithrombin differed only slightly from the corresponding parameters measured in the presence of undegraded high-affinity heparin. Moreover, the binding constants obtained for the oligosaccharides and for high-affinity heparin were similar (1.0-2.9 X 10(7) M-1 at I = 0.3). In contrast, two hexasaccharides corresponding to units 1-6 and 3-8, respectively, of the above sequence showed about a 1000-fold lower affinity for antithrombin, and also induced considerably different spectral perturbations in antithrombin. Since the 1-6 hexasaccharide contains a reducing-terminal anhydromannose residue instead of the N-sulfated glucosamine unit 6 of the intact sequence, these results strongly support our previous conclusion that the N-sulfate group at position 6 is essential to the interaction with antithrombin. The low affinity of the hexasaccharide 3-8 provides further evidence that a pentasaccharide sequence 2-6 constitutes the actual antithrombin-binding region in the heparin molecule. Structural analysis of the various oligosaccharides revealed natural variants with an N-sulfate group substituted for the N-acetyl group at position 2. The preponderance of N-acetyl over N-sulfate groups at this position may be rationalized in terms of the mechanism of heparin biosynthesis, assuming that the D-gluco configuration of unit 3 is an essential feature of the antithrombin-binding region.