Kornienko Oleg, Lacson Raul, Kunapuli Priya, Schneeweis Jonathan, Hoffman Ira, Smith Todd, Alberts Melissa, Inglese James, Strulovici Berta
Merck Research Laboratories, Department of Automated Biotechnology, North Wales, PA 19454, USA.
J Biomol Screen. 2004 Apr;9(3):186-95. doi: 10.1177/1087057103260070.
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.
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。