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Cited by 340

The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.

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

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Lindahl, U, Thunberg, L, Bäckström, G, Riesenfeld, J, Nordling, K, Björk, I·1984·Journal of Biological Chemistry

Abstract

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.

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Metadata

Authors
Lindahl, U., Thunberg, L., Bäckström, G., Riesenfeld, J., Nordling, K., & Björk, I.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1984-10
Volume
259
Issue
20
Pages
12368-12376
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1531766605
Cited by
340
References
37
FWCI
8.16
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Extension and structural variability of the antithrombin-binding sequence in heparin. https://app.cochat.ai/papers/10.1016/s0021-9258(18)90755-6
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Lindahl, U., Thunberg, L., Bäckström, G., Riesenfeld, J., Nordling, K., & Björk, I. (1984). Extension and structural variability of the antithrombin-binding sequence in heparin. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(18)90755-6

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