Illuminating the Energy Landscape of GPCRs: The Key Contribution of Solution-State NMR Associated with Escherichia coli as an Expression Host

被引:14
作者
Casiraghi, Marina [1 ]
Damian, Marjorie [2 ]
Lescop, Ewen [3 ]
Baneres, Jean-Louis [2 ]
Catoire, Laurent J. [1 ]
机构
[1] Univ Paris Diderot, Sorbonne Paris Cite, CNRS,Inst Biol Physicochim FRC 550, Lab Biol Physicochim Prot Membranaires,UMR 7099, 13 Rue Pierre & Marie Curie, F-75005 Paris, France
[2] Univ Montpellier, CNRS, IBMM, UMR5247,ENSCM, 15 Av Charles Flahault, F-34093 Montpellier, France
[3] CEA, CNRS, 1 Av Terrasse, F-91198 Gif Sur Yvette, France
关键词
PROTEIN-COUPLED RECEPTORS; MOLECULAR-WEIGHT PROTEINS; ISOTOPE LABELING STRATEGIES; MU-OPIOID RECEPTOR; MEMBRANE-PROTEINS; BETA(2)-ADRENERGIC RECEPTOR; IN-VITRO; CONFORMATIONAL-CHANGES; BINDING PROTEIN; DYNAMIC PROCESS;
D O I
10.1021/acs.biochem.8b00035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Conformational dynamics of GPCRs are central to their function but are difficult to explore at the atomic scale. Solution-state NMR has provided the major contribution in that area of study during the past decade, despite nonoptimized labeling schemes due to the use of insect cells and, to a lesser extent, yeast as the main expression hosts. Indeed, the most efficient isotope-labeling scheme ever to address energy landscape issues for large proteins or protein complexes relies on the use of (CH3)-C-13 probes immersed in a perdeuterated dipolar environment, which is essentially out of reach of eukaryotic expression systems. In contrast, although its contribution has been underestimated because of technical issues, Escherichia coli is by far the best-adapted host for such labeling. As it is now tightly controlled, we show in this review that bacterial expression can provide an NMR spectral resolution never achieved in the GPCR field.
引用
收藏
页码:2297 / 2307
页数:11
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