Abstract
Diazirine-based photoaffinity labeling is recognized as one of the most reliable methods for analyzing protein-ligand interactions. Despite its excellent chemical and physical properties, the labeling process consists of an inefficient series of analytical steps: probe preparation, detection and isolation of the target protein, and identification of the labeled site within the active site. Firstly, this review introduces a versatile method for derivatization of tri fluoromethyl phenyl diazirine, the most common photocross-linker, then discusses its use in optimizing the probe for the simplification of labeled protein analyses including selective detection and purification, and the resulting acceleration of target protein identification by structural analysis. The present review reflects recent achievements in the chemistry and biological application of diazirine photoaffinity probes.
Original language | English |
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Pages (from-to) | 2697-2727 |
Number of pages | 31 |
Journal | Heterocycles |
Volume | 89 |
Issue number | 12 |
DOIs | |
State | Published - 2014 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry