Single-Molecule Analysis of G Protein-Coupled Receptor Stoichiometry: Approaches and Limitations

被引:26
作者
Felce, James H. [1 ]
Davis, Simon J. [2 ,3 ]
Klenerman, David [4 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Oxford OX3 7FY, England
[2] Univ Oxford, Weatherall Inst Mol Med, Radcliffe Dept Med, Oxford OX3 9DS, England
[3] Univ Oxford, Weatherall Inst Mol Med, MRC, Human Immunol Unit, Oxford OX3 9DS, England
[4] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
BIMOLECULAR FLUORESCENCE COMPLEMENTATION; RESONANCE ENERGY-TRANSFER; LIVING CELLS; GPCR OLIGOMERIZATION; BETA(2)-ADRENERGIC RECEPTOR; MUSCARINIC RECEPTOR; SIGNAL-TRANSDUCTION; CARDIAC MYOCYTES; PLASMA-MEMBRANE; BRET ANALYSIS;
D O I
10.1016/j.tips.2017.10.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
How G protein-coupled receptors (GPCRs) are organized at the cell surface remains highly contentious. Single-molecule (SM) imaging is starting to inform this debate as receptor behavior can now be visualized directly, without the need for interpreting ensemble data. The limited number of SM studies of GPCRs undertaken to date have strongly suggested that dimerization is at most transient, and that most receptors are monomeric at any given time. However, even SM data has its caveats and needs to be interpreted carefully. Here, we discuss the types of SM imaging strategies used to examine GPCR stoichiometry and consider some of these caveats. We also emphasize that attempts to resolve the debate ought to rely on orthogonal approaches to measuring receptor stoichiometry.
引用
收藏
页码:96 / 108
页数:13
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