Punit Saraon, Ingrid Grozavu, Sang Hyun Lim, Jamie Snider, Zhong Yao, Igor Stagljar
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引用次数: 16
Abstract
Protein-protein interactions (PPIs) play an integral role in numerous cellular processes. Membrane protein interactions, in particular, are critical in cellular responses to stresses and stimuli, with dysfunction of these PPIs (e.g., due to aberrant expression and/or mutation of interaction partners) leading to a diverse array of pathological states. Exploration of the interaction space and dynamics of membrane proteins is difficult due to the limitations of current techniques used to study proteins in the biochemically complex environment of biological membranes. In the protocols below, we describe a newly developed membrane protein interaction assay called the Mammalian-Membrane Two-Hybrid (MaMTH), designed specifically for the detection of integral membrane PPIs in the context of living mammalian cells. Prior to using MaMTH, cell lines of interest are genetically modified to encode a reporter of choice. MaMTH “bait” and “prey” constructs of interest are also generated using Gateway cloning technology. The assay is then performed by co-transfection of baits and preys, with bait-prey interaction quantifiably assessed by way of a reporter signal (e.g., light (luciferase), fluorescence (GFP). © 2017 by John Wiley & Sons, Inc.
利用哺乳动物膜双杂交(MaMTH)试验检测膜蛋白-蛋白相互作用
蛋白质-蛋白质相互作用(PPIs)在许多细胞过程中起着不可或缺的作用。特别是膜蛋白相互作用,在细胞对应激和刺激的反应中是至关重要的,这些PPIs的功能障碍(例如,由于相互作用伙伴的异常表达和/或突变)导致各种病理状态。由于目前用于研究生物膜生物化学复杂环境中的蛋白质的技术的局限性,探索膜蛋白的相互作用空间和动力学是困难的。在下面的方案中,我们描述了一种新开发的膜蛋白相互作用试验,称为哺乳动物-膜双杂交(MaMTH),专门用于在活的哺乳动物细胞中检测整体膜PPIs。在使用MaMTH之前,对感兴趣的细胞系进行基因修饰以编码选择的报告基因。MaMTH“诱饵”和“猎物”结构感兴趣也产生使用网关克隆技术。然后通过诱饵和猎物的共转染来进行检测,通过报告信号(例如光(荧光素酶)、荧光(GFP)来定量评估诱饵-猎物相互作用。©2017 by John Wiley &儿子,Inc。
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