Measurement of Receptor Signaling Bias

Q2 Pharmacology, Toxicology and Pharmaceutics
Terry Kenakin
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引用次数: 6

Abstract

G protein–coupled receptors (GPCRs) are often pleiotropically linked to numerous cellular signaling mechanisms in cells, and it is now known that many agonists differentially activate some signaling pathways at the expense of others. The mechanism for this effect is the stabilization of different active receptor states by different agonists, and it leads to varying qualities of efficacy for different agonists. Agonist bias is a powerful mechanism to amplify beneficial signals and diminish harmful signals, and thus improve the overall profile of agonist ligands. This unit describes a method to quantify agonist bias with a scale that enables medicinal chemists to amplify or reduce these effects in new molecules. The method is based on the Black/Leff operational model and yields a statistical estimate of the confidence for bias measurements. © 2016 by John Wiley & Sons, Inc.

受体信号偏倚的测量
G蛋白偶联受体(gpcr)通常与细胞中的许多细胞信号传导机制多效相关,现在已知许多激动剂以牺牲其他信号传导途径为代价来不同地激活某些信号传导途径。这种效应的机制是不同的激动剂稳定不同的活性受体状态,这导致不同激动剂的疗效质量不同。激动剂偏置是一种强大的机制,可以放大有益信号,减少有害信号,从而改善激动剂配体的整体特征。本单元描述了一种量化激动剂偏倚的方法,该方法使药物化学家能够在新分子中放大或减少这些效应。该方法基于Black/Leff操作模型,并产生偏差测量置信度的统计估计。©2016 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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