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Originally published In Press as doi:10.1074/mcp.M600298-MCP200 on January 9, 2007.
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Molecular & Cellular Proteomics 6:835-844, 2007.
© 2007 by The American Society for Biochemistry and Molecular Biology, Inc.


Research

Purification and Identification of G Protein-coupled Receptor Protein Complexes under Native Conditions*,S

Avais M. Daulat{ddagger},§,||,**, Pascal Maurice{ddagger},§,||, Carine Froment{ddagger}{ddagger}, Jean-Luc Guillaume{ddagger},§,||, Cédric Broussard{ddagger},§,||, Bernard Monsarrat{ddagger}{ddagger},§§, Philippe Delagrange¶¶ and Ralf Jockers{ddagger},§,||,||||

From the {ddagger} Department of Cell Biology, Institut Cochin, § INSERM U567, CNRS UMR 8104, and || Faculté de Médecine René Descartes, UMR-S 8104, Université Paris Descartes, Paris F-75014, France, {ddagger}{ddagger} Institut de Biologie Structurale et de Pharmacologie, CNRS UMR 5089, Toulouse 31076, France, and ¶¶ Institut de Recherches SERVIER, Suresnes 92150, France

G protein-coupled receptors (GPCRs) constitute the largest family of membrane receptors and are of major therapeutic importance. The identification of GPCR-associated proteins is an important step toward a better understanding of these receptors. However, current methods are not satisfying as only isolated receptor domains (intracellular loops or carboxyl-terminal tails) can be used as "bait." We report here a method based on tandem affinity purification coupled to mass spectrometry that overcomes these limitations as the entire receptor is used to identify protein complexes formed in living mammalian cells. The human MT1 and MT2 melatonin receptors were chosen as model GPCRs. Both receptors were tagged with the tandem affinity purification tag at their carboxyl-terminal tails and expressed in human embryonic kidney 293 cells. Receptor solubilization and purification conditions were optimized. The method was validated by the co-purification of Gi proteins, which are well known GPCR interaction partners but which are difficult to identify with current protein-protein interaction assays. Several new and functionally relevant MT1- and MT2-associated proteins were identified; some of them were common to both receptors, and others were specific for each subtype. Taken together, our protocol allowed for the first time the purification of GPCR-associated proteins under native conditions in quantities suitable for mass spectrometry analysis.


|||| To whom correspondence should be addressed. Tel.: 331-40-51-64-34; Fax: 331-40-51-64-30; E-mail: jockers{at}cochin.inserm.fr


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