Nagai Hiroki, Kubori Tomoko
Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Methods Mol Biol. 2013;954:347-54. doi: 10.1007/978-1-62703-161-5_21.
Bacterial virulence proteins often mimic host eukaryotic proteins to modify or disturb host cellular -pathways. Increasing lines of evidence show that many bacterial effector proteins have E3 ubiquitin ligase activity. The effector protein LubX is one such bacterial E3 ubiquitin ligase. We describe here the method to purify soluble LubX protein using GST-tag and Escherichia coli overexpression systems. Using the purified protein together with recombinant ubiquitin, E1, and E2 enzymes, ubiquitin ligase activity is analyzed by the in vitro ubiquitination assay.
细菌毒力蛋白常常模仿宿主真核蛋白来修饰或干扰宿主细胞通路。越来越多的证据表明,许多细菌效应蛋白具有E3泛素连接酶活性。效应蛋白LubX就是这样一种细菌E3泛素连接酶。我们在此描述了使用GST标签和大肠杆菌过表达系统纯化可溶性LubX蛋白的方法。将纯化后的蛋白与重组泛素、E1和E2酶一起使用,通过体外泛素化试验分析泛素连接酶活性。