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从细胞内环腺苷酸变化测量看 G 蛋白偶联受体药理学;不同方法学的优缺点。

Insights into GPCR pharmacology from the measurement of changes in intracellular cyclic AMP; advantages and pitfalls of differing methodologies.

机构信息

Institute of Cell Signalling, School of Biomedical Sciences, Medical School, Queen's Medical Centre, Nottingham, UK.

出版信息

Br J Pharmacol. 2010 Nov;161(6):1266-75. doi: 10.1111/j.1476-5381.2010.00779.x.

Abstract

It is clear that the G protein-coupled receptor family play a key role in the pharmaceutical industry, with a significant proportion of approved drugs targeting this protein class. While our growing understanding of the complexity of G protein-coupled receptor pharmacology is playing a key role in the future success of these endeavours, with allosteric mechanisms now well integrated into the industrial community and G protein-independent signalling mechanisms establishing themselves as novel phenomenon to be exploited, it is still possible to underestimate the complexity of G protein signal transduction mechanisms and the impact that inappropriate study of these mechanisms can have on data interpretation. In this manuscript we review different approaches to measuring the cAMP signal transduction pathway, with particular emphasis on key parameters influencing the data quality and biological relevance.

摘要

很明显,G 蛋白偶联受体家族在制药行业中发挥着关键作用,有相当比例的已批准药物针对这一蛋白类别。尽管我们对 G 蛋白偶联受体药理学复杂性的认识不断加深,这对这些努力的未来成功起到了关键作用,变构机制现在已经很好地融入了工业界,G 蛋白非依赖性信号传导机制也确立了自身作为有待开发的新现象,但人们仍然有可能低估 G 蛋白信号转导机制的复杂性,以及对这些机制进行不当研究对数据解释的影响。在本文中,我们回顾了测量 cAMP 信号转导途径的不同方法,特别强调了影响数据质量和生物学相关性的关键参数。

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