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Enzymatic Synthesis of Chondroitin Sulfate E to Attenuate Bacteria Lipopolysaccharide-Induced Organ Damage
Author(s) -
Jine Li,
Erica Sparkenbaugh,
Guowei Su,
Fuming Zhang,
Yongmei Xu,
Ke Xia,
Pen He,
Sultan Nacak Baytaş,
Shan M. Pechauer,
Anand Padmanabhan,
Robert J. Linhardt,
Rafał Pawliński,
Jian Liu
Publication year - 2020
Publication title -
acs central science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.893
H-Index - 76
eISSN - 2374-7951
pISSN - 2374-7943
DOI - 10.1021/acscentsci.0c00712
Subject(s) - lipopolysaccharide , chondroitin sulfate , chemistry , enzyme , heparin , biochemistry , glucuronic acid , polysaccharide , chondroitin , bacteria , sulfation , inflammation , glycosaminoglycan , biology , immunology , genetics
Chondroitin sulfate E (CS-E) is a sulfated polysaccharide that contains repeating disaccharides of 4,6-disulfated N -acetylgalactosamine and glucuronic acid residues. Here, we report the enzymatic synthesis of three homogeneous CS-E oligosaccharides, including CS-E heptasaccharide ( CS-E 7-mer ), CS-E tridecasaccharide ( CS-E13-mer ), and CS-E nonadecasaccharide ( CS-E 19-mer ). The anti-inflammatory effect of CS-E 19-mer was investigated in this study. CS-E 19-mer neutralizes the cytotoxic effect of histones in a cell-based assay and in mice. We also demonstrate that CS-E 19-mer treatment improves survival and protects against organ damage in a mouse model of endotoxemia induced by bacterial lipopolysaccharide (LPS). CS-E19-mer directly interacts with circulating histones in the plasma from LPS-challenged mice. CS-E 19-mer does not display anticoagulant activity nor react with heparin-induced thrombocytopenia antibodies isolated from patients. The successful synthesis of CS-E oligosaccharides provides structurally defined carbohydrates for advancing CS-E research and offers a potential therapeutic agent to treat life-threatening systemic inflammation.

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