Suppr超能文献

用于研究单细胞中G蛋白偶联受体激活的活细胞成像技术。

Live cell imaging for studying g protein-coupled receptor activation in single cells.

作者信息

Saini Deepak Kumar, Gautam Narasimhan

机构信息

Department of Anesthesiology, Washington University School of Medicine, St Louis, MO, USA.

出版信息

Methods Mol Biol. 2010;617:191-207. doi: 10.1007/978-1-60327-323-7_16.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验