A Thiol-Ene Coupling Approach to Native Peptide Stapling and Macrocyclization

Angew Chem Int Ed Engl. 2015 Sep 7;54(37):10931-4. doi: 10.1002/anie.201503975. Epub 2015 Jul 17.


We report the discovery of a peptide stapling and macrocyclization method using thiol-ene reactions between two cysteine residues and an α,ω-diene in high yields. This new approach enabled us to selectively modify cysteine residues in native, unprotected peptides with a variety of stapling modifications for helix stabilization or general macrocyclization. We synthesized stapled Axin mimetic analogues and demonstrated increased alpha helicity upon peptide stapling. We then synthesized stapled p53 mimetic analogues using pure hydrocarbon linkers and demonstrated their abilities to block the p53-MDM2 interaction and selectively kill p53 wild-type colorectal carcinoma HCT-116 cells but not p53 null cells. In summary, we demonstrated a robust and versatile peptide stapling method that could be potentially applied to both synthetic and expressed peptides.

Keywords: bioconjugation; peptide macrocyclization; peptide stapling; thiol-ene coupling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Peptides / chemistry*
  • Sulfhydryl Compounds / chemistry*


  • Peptides
  • Sulfhydryl Compounds