Stiller Christiane, Krüger Dennis M, Brauckhoff Nicolas, Schmidt Marcel, Janning Petra, Salamon Hazem, Grossmann Tom N
Chemical Genomics Centre of the Max Planck Society, Otto-Hahn-Str. 15, 44227 Dortmund, Germany.
Technical University Dortmund , Department of Chemistry and Chemical Biology, Otto-Hahn-Str. 6, 44227 Dortmund, Germany.
ACS Chem Biol. 2017 Feb 17;12(2):504-509. doi: 10.1021/acschembio.6b01013. Epub 2017 Jan 3.
Ligand-directed reactions allow chemical transformations at very low reactant concentrations and can thus provide access to efficient approaches for the post-translational modification of proteins. The development of these proximity-induced reactions is hampered by the number of appropriate ligands and the lack of design principles. Addressing these limitations, we report a proximity-induced labeling system which applies a moderate affinity peptide ligand. The design process was structure-guided and supported by molecular dynamics simulations. We show that selective protein labeling can be performed inside living cells enabling the subcellular translocation of a protein via ligand-directed chemistry for the first time.
配体导向反应能够在极低反应物浓度下实现化学转化,从而为蛋白质的翻译后修饰提供高效方法。这些邻近诱导反应的发展受到合适配体数量以及缺乏设计原则的阻碍。为解决这些限制,我们报道了一种应用中等亲和力肽配体的邻近诱导标记系统。设计过程以结构为导向,并得到分子动力学模拟的支持。我们表明,选择性蛋白质标记可在活细胞内进行,首次实现了通过配体导向化学使蛋白质进行亚细胞转运。