Literature DB >> 15595821

Oligomerization of G protein-coupled receptors: past, present, and future.

Paul S-H Park1, Slawomir Filipek, James W Wells, Krzysztof Palczewski.   

Abstract

G protein-coupled receptor (GPCR)-mediated signal transduction has been studied for more than a century. Despite the intense focus on this class of proteins, a molecular understanding of what constitutes the functional form of the receptor is still uncertain. GPCRs have traditionally been conceptualized as monomeric proteins, and this view has changed little over the years until relatively recently. Recent biochemical and biophysical studies have challenged this traditional concept, and point instead to a mechanistic view of signal transduction wherein the receptor functions as an oligomer. Cooperative interactions within such an oligomeric array may be critical for the propagation of an external signal across the cell membrane and to the G protein, and may therefore underlie the mechanistic basis of signaling.

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Year:  2004        PMID: 15595821      PMCID: PMC1752221          DOI: 10.1021/bi047907k

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  203 in total

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  84 in total

1.  Oligomeric forms of G protein-coupled receptors (GPCRs).

Authors:  Krzysztof Palczewski
Journal:  Trends Biochem Sci       Date:  2010-06-09       Impact factor: 13.807

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Authors:  John A Salon; David T Lodowski; Krzysztof Palczewski
Journal:  Pharmacol Rev       Date:  2011-12       Impact factor: 25.468

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Journal:  J Biomed Opt       Date:  2010 Nov-Dec       Impact factor: 3.170

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Journal:  J Biol Chem       Date:  2010-12-17       Impact factor: 5.157

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Authors:  P S-H Park
Journal:  Curr Med Chem       Date:  2012       Impact factor: 4.530

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

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Journal:  J Biol Chem       Date:  2005-04-29       Impact factor: 5.157

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9.  Protease-activated receptor 1 (PAR1) and PAR4 heterodimers are required for PAR1-enhanced cleavage of PAR4 by α-thrombin.

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Journal:  J Biol Chem       Date:  2013-10-04       Impact factor: 5.157

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Authors:  Chaoyang Xue; Yen-Ping Hsueh; Joseph Heitman
Journal:  FEMS Microbiol Rev       Date:  2008-09-22       Impact factor: 16.408

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