Lundstrom Kenneth, Wagner Renaud, Reinhart Christoph, Desmyter Aline, Cherouati Nadia, Magnin Thierry, Zeder-Lutz Gabrielle, Courtot Melanie, Prual Cécile, André Nicolas, Hassaine Gherici, Michel Hartmut, Cambillau Christian, Pattus Franc
Bioxtal, Chemin des Croisettes 22, Epalinges CH-1066, Switzerland.
J Struct Funct Genomics. 2006 Jun;7(2):77-91. doi: 10.1007/s10969-006-9011-2. Epub 2006 Nov 22.
Production of recombinant receptors has been one of the major bottlenecks in structural biology on G protein-coupled receptors (GPCRs). The MePNet (Membrane Protein Network) was established to overexpress a large number of GPCRs in three major expression systems, based on Escherichia coli, Pichia pastoris and Semliki Forest virus (SFV) vectors. Evaluation by immunodetection demonstrated that 50% of a total of 103 GPCRs were expressed in bacterial inclusion bodies, 94% in yeast cell membranes and 95% in SFV-infected mammalian cells. The expression levels varied from low to high and the various GPCR families and subtypes were analyzed for their expressability in each expression system. More than 60% of the GPCRs were expressed at milligram levels or higher in one or several systems, compatible to structural biology applications. Functional activity was determined by binding assays in yeast and mammalian cells and the correlation between immunodetection and binding activity was analyzed.
重组受体的生产一直是G蛋白偶联受体(GPCRs)结构生物学研究中的主要瓶颈之一。膜蛋白网络(MePNet)的建立是为了基于大肠杆菌、巴斯德毕赤酵母和辛德毕斯病毒(SFV)载体,在三种主要表达系统中大量过表达GPCRs。通过免疫检测评估表明,在总共103种GPCRs中,50%在细菌包涵体中表达,94%在酵母细胞膜中表达,95%在SFV感染的哺乳动物细胞中表达。表达水平从低到高不等,并分析了各个GPCR家族和亚型在每个表达系统中的可表达性。超过60%的GPCRs在一个或多个系统中以毫克水平或更高水平表达,这与结构生物学应用相匹配。通过酵母和哺乳动物细胞中的结合试验测定功能活性,并分析免疫检测与结合活性之间的相关性。