Synthesis of Lipopeptides by CLipPA Chemistry

© 2021. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature..

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.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:2355

Enthalten in:

Methods in molecular biology (Clifton, N.J.) - 2355(2021) vom: 12., Seite 253-263

Sprache:

Englisch

Beteiligte Personen:

Yim, Victor [VerfasserIn]
Hermant, Yann O [VerfasserIn]
Harris, Paul W R [VerfasserIn]
Brimble, Margaret A [VerfasserIn]

Links:

Volltext

Themen:

Amino Acids
CLipPA
Cysteine
Fatty Acids
Journal Article
K848JZ4886
Lipopeptides
S-lipidation
Sulfhydryl Compounds
Thiol-ene

Anmerkungen:

Date Completed 11.01.2022

Date Revised 11.01.2022

published: Print

Citation Status MEDLINE

doi:

10.1007/978-1-0716-1617-8_19

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM329307460