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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A heparin-like glycosaminoglycan from shrimp containing high levels of 3-O-sulfated D-glucosamine groups in an unusual trisaccharide sequence

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Author(s):
Chavante, Suely F. [1] ; Brito, Adriana S. [1, 2] ; Lima, Marcelo [3, 4] ; Yates, Edwin [3, 4] ; Nader, Helena [3] ; Guerrini, Marco [5] ; Torri, Giangiacomo [5] ; Bisio, Antonella [5]
Total Authors: 8
Affiliation:
[1] Univ Fed Rio Grande do Norte, Dept Bioquim, BR-59072970 Natal, RN - Brazil
[2] Univ Fed Rio Grande do Norte, Fac Ciencias Saude Trairi, Santa Cruz, CA - USA
[3] Univ Fed Sao Paulo, Dept Bioquim, Sao Paulo - Brazil
[4] Univ Liverpool, Dept Struct & Chem Biol, Liverpool L69 3BX, Merseyside - England
[5] Ist Ric Chim & Biochim G Ronzoni, Milan - Italy
Total Affiliations: 5
Document type: Journal article
Source: Carbohydrate Research; v. 390, p. 59-66, MAY 22 2014.
Web of Science Citations: 14
Abstract

The detailed characterization of a novel heparin-like glycosaminoglycan purified from the viscera (heads) of the shrimp Litopenaeus vannamei is reported. Structural analysis performed by mono-and two-dimensional nuclear magnetic resonance (NMR) spectroscopy revealed it to be rich in both glucuronic acid and N, 6-sulfated glucosamine residues. The key peculiarities were its high 3-O-sulfated glucosamine content compared to mammalian heparins; a residue which is usually associated with the antithrombin (AT) binding site, and the location of these residues within 2-O-sulfated iduronate and glucuronate-containing sequences (I(2S-)A{*}-G), a situation not found in mammalian heparin. It also exhibited higher molecular weight (similar to 36 kDa) than conventional heparin (similar to 16 kDa) but, negligible anticoagulant activity (similar to 5 IU/mg compared to heparin similar to 190 IU/mg) and stabilization of AT, which has been linked directly to anticoagulation activity. A high affinity fraction, eluting at a similar salt concentration (0.75-1.5 M NaCl) from an antithrombin affinity column, to the high affinity fraction of heparin, also showed only weak thermal stabilization of AT (+ similar to 2 degrees C). These structural peculiarities may help elucidate more clearly the relationship between structure and function of sulfated polysaccharides, and provide useful model compounds with which to better understand interactions of biological significance. (C) 2014 Published by Elsevier Ltd. (AU)

FAPESP's process: 12/00850-1 - Bioactive compounds obtained from shrimp waste and chemical modifications of heparin
Grantee:Marcelo Andrade de Lima
Support Opportunities: Scholarships in Brazil - Post-Doctoral