| Literature DB >> 30870573 |
Brady F Cress1,2, Ujjwal Bhaskar1,2, Deepika Vaidyanathan1,2, Asher Williams1,2, Chao Cai1, Xinyue Liu1, Li Fu1, Vandhana M-Chari3,4, Fuming Zhang1, Shaker A Mousa3,4, Jonathan S Dordick1,2,5, Mattheos A G Koffas1,2,5, Robert J Linhardt1,2,5,6.
Abstract
Heparin is a highly sulfated, complex polysaccharide and widely used anticoagulant pharmaceutical. In this work, we chemoenzymatically synthesized perdeuteroheparin from biosynthetically enriched heparosan precursor obtained from microbial culture in deuterated medium. Chemical de-N-acetylation, chemical N-sulfation, enzymatic epimerization, and enzymatic sulfation with recombinant heparin biosynthetic enzymes afforded perdeuteroheparin comparable to pharmaceutical heparin. A series of applications for heavy heparin and its heavy biosynthetic intermediates are demonstrated, including generation of stable isotope labeled disaccharide standards, development of a non-radioactive NMR assay for glucuronosyl-C5-epimerase, and background-free quantification of in vivo half-life following administration to rabbits. We anticipate that this approach can be extended to produce other isotope-enriched glycosaminoglycans.Entities:
Keywords: chemoenzymatic synthesis; deuterated drugs; heparin; pharmacology; stable isotope labeling
Year: 2019 PMID: 30870573 PMCID: PMC6461503 DOI: 10.1002/anie.201900768
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336