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高通量筛选中测定 G 蛋白偶联受体药理学的 A、B、C。

The A, B, Cs of G-protein-coupled receptor pharmacology in assay development for HTS.

机构信息

HTS CoE, Pfizer Global Research and Development, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK +44(0)1304644616 ; +44(0)1304655592 ;

出版信息

Expert Opin Drug Discov. 2007 May;2(5):603-19. doi: 10.1517/17460441.2.5.603.

Abstract

G-protein-coupled receptors represent one of the most important areas of research in the pharmaceutical industry, being one of the largest druggable gene families. Recognising this fact, manufacturers have developed a huge variety of homogeneous assay technologies that facilitate the quantification of receptor ligand binding events and their downstream signalling cascades. However, while early emphasis was placed on the most sensitive, high-throughput and cost-effective screening technologies to enable identification of the most lead matter for further development, in recent years emphasis has shifted to a focus on maximising the identification of compounds that are new and developing assays that are more biologically/pharmacologically relevant. Therefore, this review provides an overview of the binding and functional techniques available for high-throughput screening, with particular attention on how assay application and configuration can be maximised to ensure their successful identification of relevant chemical matter and thereby optimising project success.

摘要

G 蛋白偶联受体是制药行业研究的重要领域之一,是最大的可成药基因家族之一。认识到这一事实,制造商开发了各种均质测定技术,以促进受体配体结合事件及其下游信号级联的定量。然而,虽然早期的重点是最敏感、高通量和具有成本效益的筛选技术,以确定最有前景的先导物质进行进一步开发,但近年来的重点已转向最大限度地识别新化合物和开发更具生物学/药理学相关性的测定方法。因此,本文综述了高通量筛选中可用的结合和功能技术,特别关注如何最大限度地应用和配置测定方法,以确保成功鉴定相关化学物质,从而优化项目成功。

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