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Updated: Jul 9, 2025

Identification of Small Molecule-binding Proteins in a Native Cellular Environment by Live-cell Photoaffinity Labeling
Published on: September 20, 2016
Evaluation of Direct Ligand-Receptor Interactions by Photoaffinity Labeling
Hidefumi Shinohara1, Yoshikatsu Matsubayashi2
1Department of Bioscience and Biotechnology, Fukui Prefectural University, Fukui, Japan.
Abstract:
Binding assays provide ultimate proof that a particular peptide and receptor kinase (RK) do indeed function as a ligand-receptor pair. Among available binding assays, proximity-induced photoaffinity labeling is superior for confirming direct contact between the peptide ligand and the receptor. Our binding assay employs covalent photoaffinity labeling followed by immunoprecipitation to specifically evaluate the ligand binding activity of the target RKs. Here, we describe a protocol for the synthesis of photoactivatable peptide ligands and the UV-induced formation of covalent bonds between photoaffinity ligands and RKs.
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