Synthesis of thioester peptides for the incorporation of thioamides into proteins by native chemical ligation

J Pept Sci. 2014 Feb;20(2):87-91. doi: 10.1002/psc.2589. Epub 2014 Jan 9.

Abstract

Thioamides can be used as photoswitches, as reporters of local environment, as inhibitors of enzymes, and as fluorescence quenchers. We have recently demonstrated the incorporation of thioamides into polypeptides and proteins using native chemical ligation (NCL). In this protocol, we describe procedures for the synthesis of a thioamide precursor and an NCL-ready thioamide-containing peptide using Dawson's N-acyl-benzimidazolinone (Nbz) process. We include a description of the synthesis by NCL of a thioamide-labeled fragment of the neuronal protein α-synuclein.

Keywords: Fmoc SPPS; Native Chemical Ligation; Thioamide; Thioester.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acylation
  • Chemistry Techniques, Synthetic*
  • Molecular Structure
  • Peptides / chemical synthesis*
  • Proteins / chemical synthesis*
  • Proteins / chemistry
  • Sulfides / chemical synthesis*
  • Sulfides / chemistry
  • Thioamides / chemistry*

Substances

  • Peptides
  • Proteins
  • Sulfides
  • Thioamides