Seeing and sensing single G protein-coupled receptors by atomic force microscopy

被引:14
作者
Sapra, K. Tanuj [1 ]
Spoerri, Patrizia M. [1 ]
Engel, Andreas [1 ]
Alsteens, David [2 ]
Mueller, Daniel [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Mattenstr 26, CH-4058 Basel, Switzerland
[2] Catholic Univ Louvain, Louvain Inst Biomol Sci & Technol, Croix Sud 4-5,Bte L7-07-07, B-1348 Louvain La Neuve, Belgium
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
CRYSTAL-STRUCTURE; ENERGY LANDSCAPES; LIGAND-FREE; RHODOPSIN; DYNAMICS; ACTIVATION; LIGHT; STATE;
D O I
10.1016/j.ceb.2018.10.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) relay extracellular information across cell membranes through a continuum of conformations that are not always captured in structures. Hence, complementary approaches are required to quantify the physical and chemical properties of the dynamic conformations linking to GPCR function. Atomic force microscopy (AFM)-based high-resolution imaging and force spectroscopy are unique methods to scrutinize GPCRs and to sense their interactions. Here, we exemplify recent AFM-based applications to directly observe the supramolecular assembly of GPCRs in native membranes, to measure the ligand-binding free-energy landscape, and how interactions modulate the structural properties of GPCRs. Common trends in GPCR function are beginning to emerge. We envision that technical developments in combining AFM with superresolution fluorescence imaging will provide insights into how cellular states modulate GPCRs and vice versa.
引用
收藏
页码:25 / 32
页数:8
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