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感应 G 蛋白偶联受体的激活。

Sensing G protein-coupled receptor activation.

机构信息

Institute of Pharmacology and Toxicology, University of Würzburg, Versbacher Strasse 9, 97078 Würzburg, Germany.

出版信息

Neuropharmacology. 2011 Jan;60(1):45-51. doi: 10.1016/j.neuropharm.2010.08.006. Epub 2010 Aug 18.

Abstract

G protein-coupled receptors (GPCRs) are the key elements of a highly regulated transduction machinery that generates different signaling outcomes to hormones and neurotransmitters. Until recently, it was assumed that diverse ligands of a given GPCR differ only in their ability to alter the balance between the OFF and the ON state of the receptor. However, it has now become evident that their activation mechanisms are more complex and that receptors presumably display distinguishable active conformational states, which are induced by different agonists and correlate to specific signaling outputs. The use of different labeling strategies to insert fluorescent labels into purified, reconstituted receptors, or into receptors in intact cells, has made it possible to sense receptor activation via changes in their fluorescence. Here, we summarize recent progress in the analysis of agonist-dependent activation mechanisms of GPCRs acquired using modern spectroscopic and crystallographic techniques.

摘要

G 蛋白偶联受体(GPCRs)是高度调控的转导机制的关键组成部分,该机制产生激素和神经递质的不同信号转导结果。直到最近,人们还认为给定 GPCR 的不同配体仅在改变受体的关闭和开启状态之间的平衡的能力上有所不同。然而,现在已经很明显,它们的激活机制更加复杂,并且受体可能显示出可区分的活性构象状态,这些状态由不同的激动剂诱导,并与特定的信号转导结果相关。使用不同的标记策略将荧光标记插入纯化的、重建的受体中,或插入完整细胞中的受体中,使得通过其荧光变化来感知受体激活成为可能。在这里,我们总结了使用现代光谱学和晶体学技术获得的 GPCR 激动剂依赖性激活机制分析方面的最新进展。

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