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« Previous AbstractModified yeast cells to investigate the coupling of G protein-coupled receptors to specific G proteins    Next AbstractDifferential effects of RGS proteins on G alpha(q) and G alpha(11) activity »

Mol Microbiol


Title:A constitutively active GPCR retains its G protein specificity and the ability to form dimers
Author(s):Ladds G; Davis K; Das A; Davey J;
Address:"Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, UK. Graham.ladds@warwick.ac.uk"
Journal Title:Mol Microbiol
Year:2005
Volume:55
Issue:2
Page Number:482 - 497
DOI: 10.1111/j.1365-2958.2004.04394.x
ISSN/ISBN:0950-382X (Print) 0950-382X (Linking)
Abstract:"G protein-coupled receptors (GPCRs) are cell surface proteins which help to regulate the physiology of all the major organ systems within higher eukaryotes. They are stimulated by multiple ligands and activate a range of effector molecules to bring about changes in cell behaviour. The use of constitutively active mutants (CAMs) of GPCRs has enabled a better understanding of receptor activation as CAMs exhibit ligand-independent signalling negating the use of ligands. Here we introduce the fission yeast Schizosaccharomyces pombe as a host for producing CAMs, by describing the isolation and characterization of constitutive mutants of the P-factor receptor (Mam2). One mutant Mam2[P261L] contained a single-amino-acid substitution (Pro261 to Leu) within a region of high homology in GPCRs. Substitution of this proline leads to an 18-fold increase in ligand-independent signalling. We utilized Mam2[P261L] to investigate CAM activity by demonstrating that Mam2[P261L] is efficiently trafficked to the cell surface where it can form fully functional oligomeric complexes with the native receptor. Mam2[P261L] also retains the G protein specificity (RG-profile) of the native receptor and only induces constitutive signalling in the same G proteins. Finally, evidence is provided to indicate that CAM activity results from a reduction in the kinetics of G protein binding. This is the first time that S. pombe has been utilized for isolating and characterizing CAMs and the techniques employed will complement the current systems available for studying these important receptors"
Keywords:"Amino Acid Sequence Cell Fractionation Cell Membrane/metabolism Dimerization Fungal Proteins Ligands Molecular Sequence Data Mutation Pheromones/*metabolism Protein Transport Receptors, G-Protein-Coupled/genetics/*metabolism Schizosaccharomyces/genetics/*;"
Notes:"MedlineLadds, Graham Davis, Kevin Das, Anamika Davey, John eng Research Support, Non-U.S. Gov't England 2005/01/22 Mol Microbiol. 2005 Jan; 55(2):482-97. doi: 10.1111/j.1365-2958.2004.04394.x"

 
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