Enzyme-catalyzed macrocyclization of long unprotected peptides

Org Lett. 2014 Jul 18;16(14):3652-5. doi: 10.1021/ol501609y. Epub 2014 Jul 8.

Abstract

A glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective S(N)Ar reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on the same polypeptide chain. Cyclic peptides ranging from 9 to 24 residues were quantitatively produced within 2 h in aqueous pH = 8 buffer at room temperature. The reaction was highly selective for cyclization at the GSH tag, enabling the combination of GST-catalyzed ligation with native chemical ligation to generate a large 40-residue peptide macrocycle.

Publication types

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

MeSH terms

  • Catalysis
  • Cyclization
  • Glutathione / chemistry*
  • Glutathione Transferase / metabolism*
  • Molecular Structure
  • Peptides / chemistry*
  • Peptides, Cyclic / chemical synthesis*
  • Peptides, Cyclic / chemistry

Substances

  • Peptides
  • Peptides, Cyclic
  • Glutathione Transferase
  • Glutathione