| Literature DB >> 31644827 |
Jun Liu1, Lingchao Cai1, Wei Sun1, Rujin Cheng2, Nanxi Wang1, Ling Jin3, Sharon Rozovsky2, Ian B Seiple1, Lei Wang1.
Abstract
Small-molecule crosslinkers are invaluable for probing biomolecular interactions and for crosslinking mass spectrometry. Existing chemical crosslinkers target only a small selection of amino acids, while conventional photo-crosslinkers target almost all residues non-specifically, complicating data analysis. Herein, we report photocaged quinone methide (PQM)-based crosslinkers that target nine nucleophilic residues through Michael addition, including Gln, Arg, and Asn, which are inaccessible to existing chemical crosslinkers. PQM crosslinkers were used in vitro, in Escherichia coli, and in mammalian cells to crosslink dimeric proteins and endogenous membrane receptors. The heterobifunctional crosslinker NHQM could crosslink proteins to DNA, for which few crosslinkers exist. The photoactivatable reactivity of these crosslinkers and their ability to target multiple amino acids will enhance the use of chemical crosslinking for studies of protein-protein and protein-DNA networks and for structural biology.Entities:
Keywords: DNA-protein interactions; crosslinker; photoaffinity labeling; protein-protein interactions; quinone methide
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Year: 2019 PMID: 31644827 PMCID: PMC6917869 DOI: 10.1002/anie.201910135
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336