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In-vivo Detection of Protein-protein Interactions on Micro-patterned Surfaces

机译:微图案化表面上蛋白质相互作用的体内检测

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摘要

Unraveling the interaction network of molecules in-vivo is key to understanding the mechanisms that regulate cell function and metabolism. A multitude of methodological options for addressing molecular interactions in cells have been developed, but most of these methods suffer from being rather indirect and therefore hardly quantitative. On the contrary, a few high-end quantitative approaches were introduced, which however are difficult to extend to high throughput. To combine high throughput capabilities with the possibility to extract quantitative information, we recently developed a new concept for identifying protein-protein interactions (Schwarzenbacher et al., 2008). Here, we describe a detailed protocol for the design and the construction of this system which allows for analyzing interactions between a fluorophore-labeled protein ("prey") and a membrane protein ("bait") in-vivo. Cells are plated on micropatterned surfaces functionalized with antibodies against the bait exoplasmic domain. Bait-prey interactions are assayed via the redistribution of the fluorescent prey. The method is characterized by high sensitivity down to the level of single molecules, the capability to detect weak interactions, and high throughput capability, making it applicable as screening tool.
机译:弄清体内分子的相互作用网络是了解调节细胞功能和代谢机制的关键。已经开发出解决细胞中分子相互作用的多种方法学选择,但是这些方法中的大多数都具有相当间接的缺点,因此难以定量。相反,引入了一些高端定量方法,但是这些方法很难扩展到高通量。为了将高通量能力与提取定量信息的可能性结合起来,我们最近开发了一种新的概念,用于识别蛋白质与蛋白质的相互作用(Schwarzenbacher等,2008)。在这里,我们描述了该系统的设计和构建的详细协议,该协议允许在体内分析荧光团标记的蛋白质(“猎物”)和膜蛋白(“诱饵”)之间的相互作用。将细胞铺在用抗诱饵胞外域抗体功能化的微图案表面上。通过荧光猎物的重新分布分析诱饵-猎物的相互作用。该方法的特点是低至单分子水平的高灵敏度,检测弱相互作用的能力和高通量的能力,使其可作为筛选工具。

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