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用于重组和内源性表达的G蛋白偶联受体药理学研究的动态质量再分布技术评估

Evaluation of dynamic mass redistribution technology for pharmacological studies of recombinant and endogenously expressed g protein-coupled receptors.

作者信息

Lee Paul H, Gao Alice, van Staden Carlo, Ly Jenny, Salon John, Xu Arron, Fang Ye, Verkleeren Ron

机构信息

Chemistry Research and Discovery, Amgen Inc., Thousand Oaks, California, USA.

出版信息

Assay Drug Dev Technol. 2008 Feb;6(1):83-94. doi: 10.1089/adt.2007.126.

Abstract

The Epic cell assay technology (Corning Inc., Corning, NY) uses a resonant waveguide grating optical biosensor to measure cellular response to ligands manifested through dynamic mass redistribution (DMR) of cellular contents. The DMR measurement is a noninvasive, label-free assay that can be used to assess the pharmacological properties of compounds. In this study, a panel of 12 compounds was evaluated against two G protein-coupled receptor (GPCR) targets in recombinant expressed cell lines using the Corning Epic system in 384-well microplates. The evaluation was performed in a double-blinded fashion such that the identity and properties of both the GPCR targets and compounds were unknown to the researchers at the time of the study. Analysis of the DMR response from cell stimulation was used to identify compounds that functioned as agonists or antagonists and to evaluate the associated efficacy and potency. DMR results were shown to have good agreement with data obtained from cyclic AMP and calcium flux assays for compounds evaluated. A further analysis was performed and successfully identified the signaling pathways that the two GPCRs activated. In addition, the DMR measurement was able to detect responses from an endogenous receptor in these cells. The Epic DMR technology provides a generic platform amenable to pharmacological evaluation of cellular responses to GPCR activation in a label-free live cell assay format.

摘要

Epic细胞分析技术(康宁公司,纽约州康宁)使用共振波导光栅光学生物传感器来测量细胞对配体的反应,这种反应通过细胞内容物的动态质量再分布(DMR)表现出来。DMR测量是一种非侵入性、无标记的分析方法,可用于评估化合物的药理特性。在本研究中,使用康宁Epic系统在384孔微孔板中,针对重组表达细胞系中的两个G蛋白偶联受体(GPCR)靶点评估了一组12种化合物。评估以双盲方式进行,使得在研究时研究人员对GPCR靶点和化合物的身份及特性均不知情。通过分析细胞刺激产生的DMR反应来鉴定作为激动剂或拮抗剂起作用的化合物,并评估相关的效力和效能。对于所评估的化合物,DMR结果与从环磷酸腺苷和钙流测定获得的数据显示出良好的一致性。进行了进一步分析并成功鉴定了两个GPCR激活的信号通路。此外,DMR测量能够检测这些细胞中内源性受体的反应。Epic DMR技术提供了一个通用平台,适用于以无标记活细胞分析形式对细胞对GPCR激活的反应进行药理评估。

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