Affiliation:
1. Sorbonne Université UFR 927 MNHN CNRS UMR 7196 INSERM U1154 43 rue Cuvier 75005 Paris France
2. Université Paris-Saclay CNRS Institut de Chimie Moléculaire et des Matériaux d'Orsay UMR CNRS 8182 91405 Orsay France
Abstract
AbstractA variety of proteins interact with DNA and RNA, including polymerases, histones, ribosomes, transcription factors, and repair enzymes. However, the transient non‐covalent nature of these interactions poses challenges for analysis. Introducing a covalent bond between proteins and DNA via photochemical activation of a photosensitive functional group introduced onto nucleic acids offers a means to stabilize these often weak interactions without significantly altering the binding interface. Consequently, photoactivatable oligonucleotides are powerful tools for investigating nucleic acid‐protein interactions involved in numerous biological and pathological processes. In this review, we provide a comprehensive overview of the chemical tools developed so far and the different strategies used for incorporating the most commonly used photoreactive reagents into oligonucleotide probes or nucleic acids. Furthermore, we illustrate their application with several examples including protein binding site mapping, identification of protein binding partners, and in cell studies.
Funder
Agence Nationale de la Recherche