Saini Deepak Kumar, Gautam Narasimhan
Department of Anesthesiology, Washington University School of Medicine, St Louis, MO, USA.
Methods Mol Biol. 2010;617:191-207. doi: 10.1007/978-1-60327-323-7_16.
G protein-coupled receptors (GPCRs) constitute the single largest family of target proteins for drugs of pain and anesthesia. Non-invasive assays based on the activity of G protein-based sensors in living cells allow the identification of potentially novel compounds for anesthesia and pain management with high specificity. Quantitative information about the efficacy of any molecule or drug compound that acts through a GPCR can be obtained through this approach. Furthermore, live cell assays provide spatio temporal information that is valuable in high content screening of compounds. Here, we describe the use of various fluorescently tagged G protein subunits and methods for using translocation and FRET-based G protein sensors in studying GPCR activation in living cells.
G蛋白偶联受体(GPCRs)是用于疼痛和麻醉药物的最大一类靶蛋白。基于活细胞中G蛋白传感器活性的非侵入性检测方法能够以高特异性鉴定出用于麻醉和疼痛管理的潜在新型化合物。通过这种方法可以获得有关任何通过GPCR起作用的分子或药物化合物功效的定量信息。此外,活细胞检测提供的时空信息在化合物的高内涵筛选中很有价值。在此,我们描述了各种荧光标记的G蛋白亚基的使用以及在研究活细胞中GPCR激活时使用基于转位和荧光共振能量转移(FRET)的G蛋白传感器的方法。