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Synthesis of the bacteriocin glycopeptide sublancin 168 and S-glycosylated variants
University of Sydney, Australia.ORCID iD: 0000-0002-0968-5793
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2012 (English)In: Organic Letters, ISSN 1523-7060, E-ISSN 1523-7052, Vol. 14, no 7, p. 1910-3Article in journal (Refereed) Published
Abstract [en]

The synthesis of sublancin 168, a unique S-glucosylated bacteriocin antibiotic, is described. The natural product and two S-glycosylated variants were successfully prepared via native chemical ligation followed by folding. The synthetic glycopeptides were shown to possess primarily an α-helical secondary structure by CD and NMR studies.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2012. Vol. 14, no 7, p. 1910-3
Keyword [en]
Native Chemical Ligation, Linked Glycopeptides, Peptide Ligation, Aqueous-Solution, Proteins, Strategy
National Category
Organic Chemistry Pharmaceutical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-211524DOI: 10.1021/ol300557gISI: 000302387800065PubMedID: 22455748Scopus ID: 2-s2.0-84859620443OAI: oai:DiVA.org:kth-211524DiVA, id: diva2:1129711
Note

QC 20170807

Available from: 2017-08-06 Created: 2017-08-06 Last updated: 2018-01-13Bibliographically approved

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