Aulakh Suraaj, Kim Kelly H, Paetzel Mark
Department of Molecular Biology and Biochemistry, Simon Fraser University, South Science Building, 8888 University Drive, Burnaby, BC, Canada, V5A 1S6.
Methods Mol Biol. 2015;1329:179-88. doi: 10.1007/978-1-4939-2871-2_14.
BamB, BamC, BamD, and BamE are lipoproteins that, along with the integral membrane protein BamA, form the β-barrel assembly machinery (BAM) complex in the outer-membrane of Gram-negative bacteria. Elucidating the roles that these lipoproteins play in the β-barrel assembly process requires both structural and functional studies that rely on milligram quantities of pure protein. Here, we describe a simple protocol for expressing individual BamB-BamE proteins in Escherichia coli and purifying them by nickel affinity and size-exclusion chromatography. This protocol yields pure proteins in amounts that are sufficient for crystallization trials, in vitro protein-protein interaction studies, NMR, and other biochemical experiments.
BamB、BamC、BamD和BamE是脂蛋白,它们与整合膜蛋白BamA一起,在革兰氏阴性菌的外膜中形成β桶组装机器(BAM)复合物。要阐明这些脂蛋白在β桶组装过程中所起的作用,需要进行结构和功能研究,而这依赖于毫克级的纯蛋白。在此,我们描述了一种在大肠杆菌中表达单个BamB - BamE蛋白并通过镍亲和色谱和尺寸排阻色谱进行纯化的简单方案。该方案可产生足够量的纯蛋白,足以用于结晶试验、体外蛋白质 - 蛋白质相互作用研究、核磁共振(NMR)及其他生化实验。