Using engineered 6-: O -sulfotransferase to improve the synthesis of anticoagulant heparin
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 18, Issue: 40, Page: 8094-8102
2020
- 9Citations
- 13Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations9
- Citation Indexes9
- CrossRef7
- Captures13
- Readers13
- 13
Article Description
Heparan sulfate (HS) and heparin are sulfated polysaccharides exhibiting diverse physiological functions. HS 6-O-sulfotransferase (6-OST) is a HS biosynthetic enzyme that transfers a sulfo group to the 6-OH position of glucosamine to synthesize HS with desired biological activities. Chemoenzymatic synthesis is a widely adopted method to obtain HS oligosaccharides to support biological studies. However, this method is unable to synthesize all possible structures due to the specificity of natural enzymes. Here, we report the use of an engineered 6-OST to achieve fine control of the 6-O-sulfation. Unlike wild type enzyme, the engineered 6-OST only sulfates the non-reducing end glucosamine residue. Utilizing the engineered enzyme and wild type enzyme, we successfully completed the synthesis of five hexasaccharides and one octasaccharide differing in 6-O-sulfation patterns. We also identified a hexasaccharide construct as a new anticoagulant drug candidate. Our results demonstrate the feasibility of using an engineered HS biosynthetic enzyme to prepare HS-based therapeutics.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85094221837&origin=inward; http://dx.doi.org/10.1039/d0ob01736a; http://www.ncbi.nlm.nih.gov/pubmed/33026409; https://xlink.rsc.org/?DOI=D0OB01736A; https://dx.doi.org/10.1039/d0ob01736a; https://pubs.rsc.org/en/content/articlelanding/2020/ob/d0ob01736a
Royal Society of Chemistry (RSC)
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