University of California, San Francisco, Department of Pharmaceutical Chemistry and the Cardiovascular Research Institute, 555 Mission Bay Blvd. South, San Francisco, CA, 94158, USA.
University of Delaware, Department of Chemistry and Biochemistry, Newark, DE, 19716, USA.
Angew Chem Int Ed Engl. 2019 Dec 19;58(52):18839-18843. doi: 10.1002/anie.201910135. Epub 2019 Nov 8.
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.
小分子交联剂对于探测生物分子相互作用和交联质谱学非常有价值。现有的化学交联剂仅针对一小部分氨基酸,而传统的光交联剂则非特异性地针对几乎所有残基,这使得数据分析变得复杂。在此,我们报告了基于光笼醌甲叉(PQM)的交联剂,它们通过迈克尔加成靶向九个亲核残基,包括 Gln、Arg 和 Asn,这些残基是现有化学交联剂无法到达的。PQM 交联剂在体外、大肠杆菌和哺乳动物细胞中用于交联二聚体蛋白和内源性膜受体。杂双功能交联剂 NHQM 可以将蛋白质与 DNA 交联,而用于 DNA 交联的交联剂很少。这些交联剂的光活化反应性及其靶向多种氨基酸的能力将增强化学交联在蛋白质-蛋白质和蛋白质-DNA 网络研究以及结构生物学中的应用。