Allene Functionalized Azobenzene Linker Enables Rapid and Light-Responsive Peptide Macrocyclization

Bioconjug Chem. 2016 Mar 16;27(3):509-14. doi: 10.1021/acs.bioconjchem.6b00026. Epub 2016 Feb 29.

Abstract

In this manuscript, we describe the efficient synthesis of a bis(allenamide) functionalized water-soluble azobenzene reagent (BSBDA) and its application as a new tool for the rapid generation of visible light-responsive macrocyclic peptides and peptide libraries displayed on the surface of bacteriophage. The allenamide functionality promotes cysteine ligation in model peptides and those displayed on phage with rates 2-3 orders of magnitude faster than the established alkyl halide containing azobenzenes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemistry*
  • Light*
  • Macrocyclic Compounds / chemistry*
  • Peptides / chemistry*

Substances

  • Azo Compounds
  • Macrocyclic Compounds
  • Peptides
  • azobenzene