| Literature DB >> 34386963 |
Victor Yim1,2, Yann O Hermant1,2, Paul W R Harris3,4,5, Margaret A Brimble6,7,8.
Abstract
Lipidation of polypeptides with a fatty acid to form N-linked lipopeptides can be a time consuming process due to the need to mask other reactive function groups present on the side chains of amino acids. Cysteine Lipidation on a Peptide or Amino acid (CLipPA) technology enables the direct lipidation of unprotected peptides containing a free thiol group to afford S-lipidated lipopeptides. A generalized procedure for the synthesis of S-lipopeptides is described which facilities rapid preparation of tens of analogs of lipopeptides from a single thiolated polypeptide precursor.Entities:
Keywords: CLipPA; Lipopeptides; S-lipidation; Thiol-ene
Mesh:
Substances:
Year: 2021 PMID: 34386963 DOI: 10.1007/978-1-0716-1617-8_19
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745