Peptidyl N,N-bis(2-mercaptoethyl)-amides as thioester precursors for native chemical ligation

Org Lett. 2011 Feb 4;13(3):386-9. doi: 10.1021/ol102735k. Epub 2010 Dec 22.

Abstract

With two β-mercaptoethyl groups on the N, a tertiary amide of structure 1 is always poised for intramolecular thioesterification however it flips about the C-N bond. It is shown that a peptide with such a C-terminal N,N-bis(2-mercaptoethyl)-amide (BMEA) can be used directly for native chemical ligation (NCL). These BMEA peptides are easily prepared with standard Fmoc-solid phase peptide synthesis protocols, thus giving a very convenient access to the thioester components for NCL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • Catalysis
  • Esters
  • Molecular Structure
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Sulfur Compounds / chemical synthesis*
  • Sulfur Compounds / chemistry

Substances

  • Amides
  • Esters
  • Peptides
  • Sulfur Compounds