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使用微量分配和检测系统对基于全活细胞的GPCR检测进行微型化。

Miniaturization of whole live cell-based GPCR assays using microdispensing and detection systems.

作者信息

Kornienko Oleg, Lacson Raul, Kunapuli Priya, Schneeweis Jonathan, Hoffman Ira, Smith Todd, Alberts Melissa, Inglese James, Strulovici Berta

机构信息

Merck Research Laboratories, Department of Automated Biotechnology, North Wales, PA 19454, USA.

出版信息

J Biomol Screen. 2004 Apr;9(3):186-95. doi: 10.1177/1087057103260070.

Abstract

Cell-based beta-lactamase reporter gene assays designed to measure the functional responses of G-protein-coupled receptors (GPCRs) were miniaturized to less than 2 microL total assay volume in a 3456-well microplate. Studies were done to evaluate both receptor agonists and antagonists. The pharmacology of agonists and antagonists for target GPCRs originally developed in a 96-well format was recapitulated in a 3456-well microplate format without compromising data quality or EC(50)/IC(50) precision. These assays were employed in high-throughput screening campaigns, allowing the testing of more than 150,000 compounds in 8 h. The instrumentation used and practical aspects of the assay development are discussed.

摘要

旨在测量G蛋白偶联受体(GPCRs)功能反应的基于细胞的β-内酰胺酶报告基因检测,在3456孔微孔板中被微型化至总检测体积小于2微升。开展了研究以评估受体激动剂和拮抗剂。最初在96孔板中开发的针对目标GPCRs的激动剂和拮抗剂的药理学,在3456孔板形式中得以重现,而不影响数据质量或EC(50)/IC(50)精度。这些检测被用于高通量筛选活动,能够在8小时内检测超过150,000种化合物。文中讨论了所使用的仪器以及检测开发的实际方面。

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