Resonance Energy Transfer-Based Approaches to Study GPCRs

被引:14
作者
Ayoub, Mohammed Akli [1 ,2 ,3 ]
机构
[1] INRA, UMR85, Unite Physiol Reprod & Comportements, Biol & Bioinformat Syst Signalisat, F-37380 Nouzilly, France
[2] CNRS, UMR7247, Nouzilly, France
[3] LE STUDIUM Loire Valley Inst Adv Studies, Orleans, France
来源
G PROTEIN-COUPLED RECEPTORS: SIGNALING, TRAFFICKING AND REGULATION | 2016年 / 132卷
关键词
PROTEIN-COUPLED-RECEPTOR; TIME-RESOLVED FLUORESCENCE; INDUCED CONFORMATIONAL-CHANGES; HETEROTRIMERIC G-PROTEINS; BETA(2) ADRENERGIC-RECEPTOR; GTP-BINDING-PROTEINS; BIOLUMINESCENCE-RESONANCE; BETA(2)-ADRENERGIC RECEPTOR; LIGAND-BINDING; TRANSFER BRET;
D O I
10.1016/bs.mcb.2015.10.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Since their discovery, G protein-coupled receptors (GPCRs) constitute one of the most studied proteins leading to important discoveries and perspectives in terms of their biology and implication in physiology and pathophysiology. This is mostly linked to the remarkable advances in the development and application of the biophysical resonance energy transfer (RET)-based approaches, including bioluminescence and fluorescence resonance energy transfer (BRET and FRET, respectively). Indeed, BRET and FRET have been extensively applied to study different aspects of GPCR functioning such as their activation and regulation either statically or dynamically, in real-time and intact cells. Consequently, our view on GPCRs has considerably changed opening new challenges for the study of GPCRs in their native tissues in the aim to get more knowledge on how these receptors control the biological responses. Moreover, the technological aspect of this field of research promises further developments for robust and reliable new RET-based assays that may be compatible with high-throughput screening as well as drug discovery programs.
引用
收藏
页码:255 / 292
页数:38
相关论文
共 243 条
[1]
Molecular mechanisms and therapeutical implications of intramembrane receptor/receptor interactions among heptahelical receptors with examples from the striatopallidal GABA neurons [J].
Agnati, LF ;
Ferré, S ;
Lluis, C ;
Franco, R ;
Fuxe, K .
PHARMACOLOGICAL REVIEWS, 2003, 55 (03) :509-550
[2]
Albizu L, 2010, NAT CHEM BIOL, V6, P587, DOI [10.1038/NCHEMBIO.396, 10.1038/nchembio.396]
[3]
Detection of β2-adrenergic receptor dimerization in living cells using bioluminescence resonance energy transfer (BRET) [J].
Angers, S ;
Salahpour, A ;
Joly, E ;
Hilairet, S ;
Chelsky, D ;
Dennis, M ;
Bouvier, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3684-3689
[4]
Biochemical and biophysical demonstration of GPCR oligomerization in mammalian cells [J].
Angers, S ;
Salahpour, A ;
Bouvier, M .
LIFE SCIENCES, 2001, 68 (19-20) :2243-2250
[5]
Dimerization: An emerging concept for G protein-coupled receptor ontogeny and function [J].
Angers, S ;
Salahpour, A ;
Bouvier, M .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2002, 42 :409-435
[6]
[Anonymous], 2006, CURR PROTOC NEUROSCI
[7]
The chemokine CXC4 and CC2 receptors form homo- and heterooligomers that can engage their signaling G-protein effectors and βarrestin [J].
Armando, Sylvain ;
Quoyer, Julie ;
Lukashova, Viktorya ;
Maiga, Arhamatoulaye ;
Percherancier, Yann ;
Heveker, Nikolaus ;
Pin, Jean-Philippe ;
Prezeau, Laurent ;
Bouvier, Michel .
FASEB JOURNAL, 2014, 28 (10) :4509-4523
[8]
Characterization of Three Vasopressin Receptor 2 Variants: An Apparent Polymorphism (V266A) and Two Loss-of-Function Mutations (R181C and M311V) [J].
Armstrong, Stephen P. ;
Seeber, Ruth M. ;
Ayoub, Mohammed Akli ;
Feldman, Brian J. ;
Pfleger, Kevin D. G. .
PLOS ONE, 2013, 8 (06)
[9]
Bioluminescence resonance energy transfer assays reveal ligand-specific conformational changes within preformed signaling complexes containing δ-opioid receptors and heterotrimeric G proteins [J].
Audet, Nicolas ;
Gales, Celine ;
Archer-Lahlou, Elodie ;
Vallieres, Marc ;
Schiller, Peter W. ;
Bouvier, Michel ;
Pineyro, Graciela .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (22) :15078-15088
[10]
Preferential formation of MT1/MT2 melatonin receptor heterodimers with distinct ligand interaction properties compared with MT2 homodimers [J].
Ayoub, MA ;
Levoye, A ;
Delagrange, P ;
Jockers, R .
MOLECULAR PHARMACOLOGY, 2004, 66 (02) :312-321