Tandem photoaffinity labeling-bioorthogonal conjugation in medicinal chemistry

Bioorg Med Chem. 2012 Nov 1;20(21):6237-47. doi: 10.1016/j.bmc.2012.09.010. Epub 2012 Sep 13.

Abstract

Photoaffinity labeling has a longstanding history as a powerful biochemical technique. However, photoaffinity labeling has significantly evolved over the past decade principally due to its coupling with bioorthogonal/click chemistry reactions. This review aims to highlight tandem photoaffinity labeling-bioorthogonal conjugation as a chemical approach in medicinal chemistry and chemical biology. In particular, recent examples of using this strategy for affinity-based protein profiling (AfBPP), drug target identification, binding ensemble profiling, studying endogenous biological molecules, and imaging applications will be presented. Additionally, recent advances in the development of 'all-in-one' compact moieties possessing a photoreactive group and clickable handle will be discussed.

Publication types

  • Review

MeSH terms

  • Chemistry, Pharmaceutical*
  • Click Chemistry
  • Photoaffinity Labels*

Substances

  • Photoaffinity Labels