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检测活细胞中 Gαi 介导的 cAMP 减少的分析方法。

Assay for Detecting Gαi-Mediated Decreases in cAMP in Living Cells.

机构信息

1 Montana Molecular, Bozeman, MT, USA.

2 Department of Photobiology and Bioimaging, The Scintillon Institute, San Diego, CA, USA.

出版信息

SLAS Discov. 2018 Oct;23(9):898-906. doi: 10.1177/2472555218786238. Epub 2018 Jul 10.

Abstract

Cell-based assays to detect Gαi signaling are often indirect, frequently involve complex pharmacological interventions, and are usually blind to the kinetics of the signaling. Our goal was to develop a simple, direct measure of Gαi signaling in living cells. We previously reported our fluorescent cADDis assay and showed that it reliably detects Gαs-mediated increases in cAMP levels. Agonists that stimulate a Gs-coupled receptor produce changes in the intensity of bright green or red fluorescent protein sensors that can be followed over time using automated fluorescence plate readers or fluorescence imaging systems. Since the cADDis sensors can monitor Gαs-mediated increases in adenylyl cyclase activity, in theory they should also be capable of detecting Gαi-mediated decreases. Here we apply our green fluorescent cADDis sensor to the detection of Gαi-mediated inhibition of adenylyl cyclase activity. We validated and optimized the assay in living HEK 293T cells using several known Gαi-coupled receptors and agonists, and we report robust Z' statistics and consistent EC responses.

摘要

基于细胞的测定法常用于检测 Gαi 信号,通常是间接的,涉及复杂的药理学干预,并且通常无法了解信号的动力学。我们的目标是开发一种简单、直接的方法来测量活细胞中的 Gαi 信号。我们之前报道了我们的荧光 cADDis 测定法,并表明它可靠地检测到 Gαs 介导的 cAMP 水平增加。刺激 Gs 偶联受体的激动剂会引起明亮的绿色或红色荧光蛋白传感器强度的变化,这些变化可以使用自动化荧光平板读数器或荧光成像系统随时间进行跟踪。由于 cADDis 传感器可以监测 Gαs 介导的腺苷酸环化酶活性的增加,因此理论上它们也应该能够检测到 Gαi 介导的减少。在这里,我们将绿色荧光 cADDis 传感器应用于检测 Gαi 介导的腺苷酸环化酶活性抑制。我们使用几种已知的 Gαi 偶联受体和激动剂在活 HEK 293T 细胞中验证和优化了该测定法,并报告了稳健的 Z'统计数据和一致的 EC 响应。

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