Photoisomerization-enhanced 1,3-dipolar cycloaddition of carbon-bridged octocyclic azobenzene with photo-released nitrile imine for peptide stapling and imaging in live cells

Org Biomol Chem. 2020 Aug 7;18(29):5602-5607. doi: 10.1039/d0ob01027h. Epub 2020 Jul 10.

Abstract

A photo-induced 1,3-dipolar cycloaddition between nitrile imine and highly ring-strained N[double bond, length as m-dash]N double bond as a dipolarophile was discovered. The photo-isomerization of carbon-bridged octocyclic azobenzene (CBOA) into its trans-configuration accelerates the ligation reaction at a very rapid rate (28 400 M-1 s-1). The CBOA-based photo-click reaction was proved to be bioorthogonal. In addition, the NoxaB peptide was successfully cross-linked by a CBOA stapler which plays a dual role: photo-control of the conformation of the peptide and photo-conjugation of probes in live cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemical synthesis*
  • Azo Compounds / chemistry
  • Carbon / chemistry*
  • Cycloaddition Reaction
  • HeLa Cells
  • Humans
  • Imines / chemistry*
  • Molecular Structure
  • Nitriles / chemistry*
  • Optical Imaging*
  • Peptides / analysis*
  • Photochemical Processes
  • Stereoisomerism

Substances

  • Azo Compounds
  • Imines
  • Nitriles
  • Peptides
  • Carbon
  • azobenzene