Opefi Chikwado A, Tranter Dale, Smith Steven O, Reeves Philip J
Department of Biological Sciences, University of Essex, Colchester, Essex, United Kingdom.
Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, USA.
Methods Enzymol. 2015;556:283-305. doi: 10.1016/bs.mie.2014.12.020. Epub 2015 Mar 20.
The large-scale expression of many membrane proteins, including the members of the G protein-coupled receptor superfamily, in a correctly folded and fully functional form remains a formidable challenge. In this chapter, we focus on the construction of stable mammalian cell lines to overcome this hurdle. First, we will outline the steps for establishing a tightly regulated gene expression system in human HEK293S cells. This system utilizes separate plasmids containing components of well-defined genetic control elements from the Escherichia coli tetracycline operon to control the powerful cytomegalovirus immediate early enhancer/promoter. Next, we describe the assembly of this expression system into HEK293S cells and a derivative cell line devoid of complex N-glycosylation. Finally, we describe methods for the growth of these cells lines in scalable suspension culture for the preparation of milligram amounts of recombinant protein.
包括G蛋白偶联受体超家族成员在内的许多膜蛋白以正确折叠且功能完整的形式进行大规模表达,仍然是一项艰巨的挑战。在本章中,我们将重点介绍构建稳定的哺乳动物细胞系以克服这一障碍。首先,我们将概述在人HEK293S细胞中建立严格调控的基因表达系统的步骤。该系统利用来自大肠杆菌四环素操纵子的含有明确遗传控制元件的单独质粒,来控制强大的巨细胞病毒立即早期增强子/启动子。接下来,我们描述将该表达系统组装到HEK293S细胞和缺乏复杂N-糖基化的衍生细胞系中的过程。最后,我们描述在可扩展的悬浮培养中培养这些细胞系以制备毫克量重组蛋白的方法。