Literature DB >> 18824244

Physiological relevance of GPCR oligomerization and its impact on drug discovery.

Rosemarie Panetta1, Michael T Greenwood.   

Abstract

The potentially large functional and physiological diversity of G-protein coupled receptor (GPCR) dimers has generated a great deal of excitement about the opportunity that dimerization provides for enabling novel drug discovery. The discovery of physiologically relevant GPCR dimers suggests that new drug targets for diseases such as schizophrenia and pre-eclampsia can be developed by targeting dimers. Most of the previous work on GPCR dimers made use of the overexpression of differentially tagged GPCRs in heterologous cell systems. Current emphasis on the development of physiologically relevant cell systems that endogenously express the appropriate combination of GPCR dimers and accessory proteins is leading to dramatic increases in our understanding of GPCR dimers. These and other new tools such as GPCR-specific antibodies will be required to develop GPCR dimer specific drugs. Given that ligands are available for only a small percentage of the large number of potentially druggable GPCRs, the use of GPCR dimers might provide the necessary targets to increase the breadth and depth of receptors available for therapeutic interventions.

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Year:  2008        PMID: 18824244     DOI: 10.1016/j.drudis.2008.09.002

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  24 in total

1.  Evidence that prokineticin receptor 2 exists as a dimer in vivo.

Authors:  Sara Marsango; Maria Carmela Bonaccorsi di Patti; Donatella Barra; Rossella Miele
Journal:  Cell Mol Life Sci       Date:  2010-12-14       Impact factor: 9.261

2.  GPCR-OKB: the G Protein Coupled Receptor Oligomer Knowledge Base.

Authors:  George Khelashvili; Kevin Dorff; Jufang Shan; Marta Camacho-Artacho; Lucy Skrabanek; Bas Vroling; Michel Bouvier; Lakshmi A Devi; Susan R George; Jonathan A Javitch; Martin J Lohse; Graeme Milligan; Richard R Neubig; Krzysztof Palczewski; Marc Parmentier; Jean-Philippe Pin; Gerrit Vriend; Fabien Campagne; Marta Filizola
Journal:  Bioinformatics       Date:  2010-05-25       Impact factor: 6.937

3.  Cholesterol modulates the dimer interface of the β₂-adrenergic receptor via cholesterol occupancy sites.

Authors:  Xavier Prasanna; Amitabha Chattopadhyay; Durba Sengupta
Journal:  Biophys J       Date:  2014-03-18       Impact factor: 4.033

4.  The oligomeric state sets GABA(B) receptor signalling efficacy.

Authors:  Laëtitia Comps-Agrar; Julie Kniazeff; Lenea Nørskov-Lauritsen; Damien Maurel; Martin Gassmann; Nathalie Gregor; Laurent Prézeau; Bernhard Bettler; Thierry Durroux; Eric Trinquet; Jean-Philippe Pin
Journal:  EMBO J       Date:  2011-05-06       Impact factor: 11.598

5.  Heteromultimerization of cannabinoid CB(1) receptor and orexin OX(1) receptor generates a unique complex in which both protomers are regulated by orexin A.

Authors:  Richard J Ward; John D Pediani; Graeme Milligan
Journal:  J Biol Chem       Date:  2011-09-09       Impact factor: 5.157

Review 6.  Progress in elucidating the structural and dynamic character of G Protein-Coupled Receptor oligomers for use in drug discovery.

Authors:  A Bortolato; J C Mobarec; D Provasi; M Filizola
Journal:  Curr Pharm Des       Date:  2009       Impact factor: 3.116

7.  Changes in conformation at the cytoplasmic ends of the fifth and sixth transmembrane helices of a yeast G protein-coupled receptor in response to ligand binding.

Authors:  George K E Umanah; Li-Yin Huang; Julianna M Maccarone; Fred Naider; Jeffrey M Becker
Journal:  Biochemistry       Date:  2011-07-12       Impact factor: 3.162

8.  Cross-desensitization and cointernalization of H1 and H2 histamine receptors reveal new insights into histamine signal integration.

Authors:  Natalia Alonso; Natalia Fernandez; Cintia Notcovich; Federico Monczor; May Simaan; Alberto Baldi; J Silvio Gutkind; Carlos Davio; Carina Shayo
Journal:  Mol Pharmacol       Date:  2013-03-05       Impact factor: 4.436

9.  Biased suppression of TP homodimerization and signaling through disruption of a TM GxxxGxxxL helical interaction motif.

Authors:  Alexander J Frey; Salam Ibrahim; Scott Gleim; John Hwa; Emer M Smyth
Journal:  J Lipid Res       Date:  2013-03-14       Impact factor: 5.922

10.  Scalable rule-based modelling of allosteric proteins and biochemical networks.

Authors:  Julien F Ollivier; Vahid Shahrezaei; Peter S Swain
Journal:  PLoS Comput Biol       Date:  2010-11-04       Impact factor: 4.475

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