Traceless synthesis of protein thioesters using enzyme-mediated hydrazinolysis and subsequent self-editing of the cysteinyl prolyl sequence

Chem Commun (Camb). 2019 Jun 21;55(49):7029-7032. doi: 10.1039/c9cc03583d. Epub 2019 May 29.

Abstract

A traceless thioester-producing protocol featuring carboxypeptidase Y-mediated hydrazinolysis of cysteinyl prolyl leucine-tagged peptides has been developed. The hydrazinolysis followed by thioesterification affords cysteinyl prolyl thioesters. Self-editing of the tag and subsequent trans-thioesterification yields peptide thioesters. The developed protocol was successfully applied to the conversion of recombinant proteins to thioesters.

MeSH terms

  • Carboxypeptidases / metabolism*
  • Cysteine / chemistry
  • Cysteine / metabolism*
  • Esters / chemistry
  • Esters / metabolism*
  • Hydrazines / chemistry
  • Hydrazines / metabolism*
  • Molecular Conformation
  • Sulfhydryl Compounds / chemistry
  • Sulfhydryl Compounds / metabolism*

Substances

  • Esters
  • Hydrazines
  • Sulfhydryl Compounds
  • Carboxypeptidases
  • Cysteine