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

被引:47
作者
Hill, Stephen J. [1 ]
Williams, Christine [2 ]
May, Lauren T. [1 ]
机构
[1] Queens Med Ctr, Sch Med, Inst Cell Signalling, Sch Biomed Sci, Nottingham NG7 2UH, England
[2] Pfizer Global Res & Dev, Sandwich, Kent, England
基金
英国医学研究理事会;
关键词
cAMP; signalling; G protein-coupled receptor; screen; drug discovery; RESONANCE ENERGY-TRANSFER; TRANSCRIPTIONAL REGULATION; GENE-TRANSCRIPTION; PROVIDE EVIDENCE; EPAC ACTIVATION; AGONIST ACTIONS; BETA-BLOCKERS; CAMP; CELLS; RECEPTORS;
D O I
10.1111/j.1476-5381.2010.00779.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:1266 / 1275
页数:10
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