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用于G蛋白偶联受体内化的细胞成像分析:在高通量筛选中的应用

Cell imaging assays for G protein-coupled receptor internalization: application to high-throughput screening.

作者信息

Lee Seungtaek, Howell Bonnie, Kunapuli Priya

机构信息

Department of Automated Biotechnology, North Wales, Pennsylvania, USA.

出版信息

Methods Enzymol. 2006;414:79-98. doi: 10.1016/S0076-6879(06)14006-9.

Abstract

There are a number of assays currently available to study G protein-coupled receptors (GPCRs), including ligand binding and functional assays. The latter category, albeit more complex, offers some obvious advantages over traditional ligand-binding assays. Functional cell-based assays typically include second messenger and reporter gene assays, which depend directly or indirectly on the cellular signaling cascade initiated upon receptor activation, respectively. More recently, cell imaging assays monitoring receptor trafficking are becoming increasingly popular. These assays, described in greater detail in this chapter, are independent of receptor signaling and are thus ideally suited for orphan receptors. In addition, these assays provide a valuable measure of receptor desensitization, an important feature for the use of GPCR agonists as potential therapeutic agents. The most popular GPCR imaging assays are based on the principles of receptor desensitization and internalization monitored directly or indirectly by green fluorescent protein.

摘要

目前有许多检测方法可用于研究G蛋白偶联受体(GPCR),包括配体结合检测和功能检测。后一类检测虽然更为复杂,但与传统的配体结合检测相比具有一些明显的优势。基于细胞的功能检测通常包括第二信使检测和报告基因检测,它们分别直接或间接依赖于受体激活后启动的细胞信号级联反应。最近,监测受体转运的细胞成像检测越来越受欢迎。本章将更详细地描述这些检测方法,它们独立于受体信号传导,因此非常适合孤儿受体。此外,这些检测方法提供了一种有价值的受体脱敏测量方法,这是将GPCR激动剂用作潜在治疗药物的一个重要特征。最流行的GPCR成像检测是基于通过绿色荧光蛋白直接或间接监测的受体脱敏和内化原理。

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