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Intramolecular and Intermolecular FRET Sensors for GPCRs – Monitoring Conformational Changes and Beyond

机译:用于GPCR的分子内和分子间褶皱传感器 - 监测构象变化及更远

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摘要

Within the past decade, a large increase in structural knowledge from crystallographic studies has significantly fostered our understanding of the structural biology of G protein-coupled receptors (GPCRs). However, information on dynamic events upon receptor activation or deactivation is not yet readily accessed by these structural approaches. GPCR-based fluorescence resonance energy transfer or bioluminescence resonance energy transfer sensors or sensors for interacting proteins (e.g., G proteins or arrestins) can in part cover this gap. The principal design of such sensors was reported 15 years ago. Since then, sensors for almost 20 different GPCRs have been designed. If used with necessary controls and cautious interpretation, such sensors can contribute significantly to our understanding of the basic mechanisms of GPCR function and beyond. In this review, we will discuss the recent developments in this area of GPCR dynamics.
机译:在过去十年中,来自晶体研究的结构知识大大增加了我们对G蛋白偶联受体(GPCR)的结构生物学的理解。 然而,关于受体激活或停用时动态事件的信息尚未通过这些结构方法容易地访问。 基于GPCR的荧光共振能量转移或生物发光共振能量传递传感器或用于相互作用(例如,G蛋白或雷丝)的传感器可以部分地覆盖该间隙。 如15年前报道了这种传感器的主要设计。 从那时起,已经设计了几乎20个不同GPCR的传感器。 如果使用必要的控制和谨慎的解释,这种传感器可以显着贡献我们对GPCR功能基本机制及超越的理解。 在本次审查中,我们将讨论GPCR动力学该领域的最新发展。

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