Zimmermann Mirjam, Cal Ruben, Janett Elia, Hoffmann Viktor, Bochet Christian G, Constable Edwin, Beaufils Florent, Wymann Matthias P
University of Basel, Department of Biomedicine, Mattenstrasse 28, Basel (Switzerland).
Angew Chem Int Ed Engl. 2014 Apr 25;53(18):4717-20. doi: 10.1002/anie.201310969. Epub 2014 Mar 26.
Chemical inducers of dimerization (CIDs) have been developed to orchestrate protein dimerization and translocation. Here we present a novel photocleavable HaloTag- and SNAP-tag-reactive CID (MeNV-HaXS) with excellent selectivity and intracellular reactivity. Excitation at 360 nm cleaves the methyl-6-nitroveratryl core of MeNV-HaXS. MeNV-HaXS covalently links HaloTag- and SNAP-tag fusion proteins, and enables targeting of selected membranes and intracellular organelles. MeNV-HaXS-mediated translocation has been validated for plasma membrane, late endosomes, lysosomes, Golgi, mitochondria, and the actin cytoskeleton. Photocleavage of MeNV-HaXS liberates target proteins and provides access to optical manipulation of protein relocation with high spatiotemporal and subcellular precision. MeNV-HaXS supports kinetic studies of protein dynamics and the manipulation of subcellular enzyme activities, which is exemplified for Golgi-targeted cargo and the assessment of nuclear import kinetics.
二聚化化学诱导剂(CIDs)已被开发用于调控蛋白质二聚化和易位。在此,我们展示了一种新型的可光裂解的卤代标签和SNAP标签反应性CID(MeNV-HaXS),它具有出色的选择性和细胞内反应活性。在360nm波长下激发可裂解MeNV-HaXS的甲基-6-硝基藜芦基核心。MeNV-HaXS可共价连接卤代标签和SNAP标签融合蛋白,并能够靶向特定的膜和细胞内细胞器。MeNV-HaXS介导的易位已在质膜、晚期内体、溶酶体、高尔基体、线粒体和肌动蛋白细胞骨架中得到验证。MeNV-HaXS的光裂解可释放靶蛋白,并提供对蛋白质重新定位进行光学操纵的途径,具有高时空和亚细胞精度。MeNV-HaXS支持蛋白质动力学的动力学研究以及亚细胞酶活性的操纵,以高尔基体靶向货物和核输入动力学评估为例。