| Literature DB >> 17120110 |
Kenneth Lundstrom1, Renaud Wagner, Christoph Reinhart, Aline Desmyter, Nadia Cherouati, Thierry Magnin, Gabrielle Zeder-Lutz, Melanie Courtot, Cécile Prual, Nicolas André, Gherici Hassaine, Hartmut Michel, Christian Cambillau, Franc Pattus.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17120110 DOI: 10.1007/s10969-006-9011-2
Source DB: PubMed Journal: J Struct Funct Genomics ISSN: 1345-711X