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标记和单分子方法监测 G 蛋白偶联受体动力学。

Labeling and Single-Molecule Methods To Monitor G Protein-Coupled Receptor Dynamics.

机构信息

Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University , 1230 York Avenue, New York, New York 10065, United States.

出版信息

Chem Rev. 2017 Jan 11;117(1):186-245. doi: 10.1021/acs.chemrev.6b00084. Epub 2016 Jun 24.

Abstract

The superfamily of G protein-coupled receptors (GPCRs) mediates a wide range of physiological responses and serves as an important category of drug targets. Earlier biochemical and biophysical studies have shown that GPCRs exist temporally in an ensemble of interchanging conformations. Single-molecule techniques are ideally suited to understand the dynamic signaling and conformational complexity of G protein-coupled receptors (GPCRs). Here, we review the progress in single-molecule studies on GPCRs. We introduce the fundamental technical aspects of single-molecule fluorescence. We also survey the methodologies for labeling GPCRs with biophysical probes, particularly fluorescent dyes, and highlight the relevant chemical biology innovations that can be instrumental for studying GPCRs. Finally, we illustrate how the optical techniques and the labeling schemes have been combined to investigate GPCR signaling and dynamics at the single-molecule level.

摘要

G 蛋白偶联受体(GPCRs)超家族介导广泛的生理反应,并作为重要的药物靶点类别。早期的生化和生物物理研究表明,GPCR 暂时存在于相互转换构象的集合中。单分子技术非常适合理解 G 蛋白偶联受体(GPCR)的动态信号和构象复杂性。在这里,我们回顾了单分子研究 GPCR 的进展。我们介绍了单分子荧光的基本技术方面。我们还调查了用生物物理探针标记 GPCR 的方法,特别是荧光染料,并强调了对研究 GPCR 至关重要的相关化学生物学创新。最后,我们说明了如何将光学技术和标记方案结合起来,在单分子水平上研究 GPCR 信号转导和动力学。

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