激酶筛选在GPCR药物发现中的新作用。

Ronald I W Osmond, Michael F Crouch, Vincent J Dupriez
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引用次数: 0

摘要

gpcr是一大类细胞表面受体,参与多种生物过程,包括许多对疾病至关重要的生物过程。因此,gpcr是药物发现研究的主要焦点,并且高度适合于治疗干预。然而,迄今为止的成功可能代表“低挂的果实”(即最容易实现的结果)。许多gpcr的信号传导现在被认为比最初认为的要复杂得多。因此,用于早期药物发现的单一gpcr介导的次级信使的传统分析,例如Ca2+的测量或cAMP的形成,可能无法提供有关靶受体的所有相关信号信息或潜在药物的所有作用的信息。考虑到这种复杂性,确定其他信号事件,如GPCR介导的主要激酶途径(包括PI3K和MAPK)的激活,可能在鉴定GPCR功能指标中变得越来越重要。此外,用于检测gpcr介导的蛋白激酶靶点激活的高效检测方法的出现,使得这类靶点易于适用于基于细胞的高通量筛选程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An emerging role for kinase screening in GPCR drug discovery.

GPCRs are a large class of cell-surface receptors that are involved in a diverse array of biological processes, including many that are critical to diseases. As a result, GPCRs are a major focus for drug discovery research, and have been highly amenable to therapeutic intervention. However, the successes to date may represent the 'low-hanging fruit' (ie, outcomes that have been easiest to achieve). The signaling of many GPCRs is now recognized to be substantially more complex than initially thought. Thus, the traditional analysis of single GPCR-mediated secondary messengers for early-stage drug discovery, such as the measurement of Ca2+ or the formation of cAMP, may not provide all of the relevant signaling information on a target receptor or information on all of the effects of potential drugs. Given this complexity, the determination of other signaling events, such as the GPCR-mediated activation of major kinase pathways, including PI3K and MAPK, is likely to become increasingly important in the identification of indicators of GPCR function. Furthermore, the advent of highly efficient assays for detecting the GPCR-mediated activation of protein kinase targets allows this target class to be readily amenable to cell-based high-throughput screening programs.

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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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