Literature DB >> 17120110

Structural genomics on membrane proteins: comparison of more than 100 GPCRs in 3 expression systems.

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.

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Year:  2006        PMID: 17120110     DOI: 10.1007/s10969-006-9011-2

Source DB:  PubMed          Journal:  J Struct Funct Genomics        ISSN: 1345-711X


  28 in total

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Review 6.  The impact of GPCR structures on pharmacology and structure-based drug design.

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