Illuminating insights into protein-protein interactions using bioluminescence resonance energy transfer (BRET)

被引:384
作者
Pfleger, KDG [1 ]
Eidne, KA
机构
[1] Univ Western Australia, Western Australian Inst Med Res, Lab Mol Endocrinol, Lab 7TM, Perth, WA 6009, Australia
[2] Univ Western Australia, UWA Ctr Med Res, Perth, WA 6009, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1038/nmeth841
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bioluminescence resonance energy transfer (BRET) is a straightforward biophysical technique for studying protein-protein interactions. It requires: (1) that proteins of interest and suitable controls be labeled with either a donor or acceptor molecule, (2) placement of these labeled proteins in the desired environment for assessing their potential interaction, and (3) use of suitable detection instrumentation to monitor resultant energy transfer. There are now several possible applications, combinations of donor and acceptor molecules, potential assay environments and detection system perturbations. Therefore, this review aims to demystify and clarify the important aspects of the BRET methodology that should be considered when using this technique.
引用
收藏
页码:165 / +
页数:10
相关论文
共 46 条
[1]   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
[2]   Detection of protein-protein interaction by bioluminescence resonance energy transfer from firefly luciferase to red fluorescent protein [J].
Arai, R ;
Nakagawa, H ;
Kitayama, A ;
Ueda, H ;
Nagamune, T .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2002, 94 (04) :362-364
[3]   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
[4]   Monitoring of ligand-independent dimerization and ligand-induced conformational changes of melatonin receptors in living cells by bioluminescence resonance energy transfer [J].
Ayoub, MA ;
Couturier, C ;
Lucas-Meunier, E ;
Angers, S ;
Fossier, P ;
Bouvier, M ;
Jockers, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :21522-21528
[5]   The BRET2/arrestin assay in stable recombinant cells:: A platform to screen for compounds that interact with G protein-coupled receptors (GPCRS) [J].
Bertrand, L ;
Parent, S ;
Caron, M ;
Legault, M ;
Joly, E ;
Angers, S ;
Bouvier, M ;
Brown, M ;
Houle, B ;
Ménard, L .
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH, 2002, 22 (1-4) :533-541
[6]   The use of resonance energy transfer in high-throughput screening: BRET versus FRET [J].
Boute, N ;
Jockers, R ;
Issad, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (08) :351-354
[7]   Hetero-oligomerization between β2-and β3-adrenergic receptors generates a β-adrenergic signaling unit with distinct functional properties [J].
Breit, A ;
Lagacé, M ;
Bouvier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (27) :28756-28765
[8]   FACS-optimized mutants of the green fluorescent protein (GFP) [J].
Cormack, BP ;
Valdivia, RH ;
Falkow, S .
GENE, 1996, 173 (01) :33-38
[9]   Activation of the leptin receptor by a ligand-induced conformational change of constitutive receptor dimers [J].
Couturier, C ;
Jockers, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (29) :26604-26611
[10]   Noninvasive imaging of protein-protein interactions from live cells and living subjects using bioluminescence resonance energy transfer [J].
De, A ;
Gambhir, SS .
FASEB JOURNAL, 2005, 19 (12) :2017-+