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来自转染细胞的免疫共沉淀。

Co-immunoprecipitation from transfected cells.

作者信息

Masters Shane C

机构信息

Medical College of Georgia, Augusta, GA, USA.

出版信息

Methods Mol Biol. 2004;261:337-50. doi: 10.1385/1-59259-762-9:337.

Abstract

One of the most commonly used methods for determining whether two proteins can interact is co-immunoprecipitation. Co-immunoprecipitation relies on the ability of an antibody to stably and specifically bind complexes containing a bait protein. The antibody provides a means of immobilizing these complexes on a solid matrix, which in the protocol presented here is accomplished through interaction with Protein A, so that irrelevant proteins can be washed away. The presence of target proteins in the bait complexes is determined by Western blot. Because of the biochemical diversity of protein-protein interactions, it is not possible to describe a single set of conditions that will work for every immunoprecipitation experiment. Instead, the goal of this chapter is to provide practical starting conditions for co-immunoprecipitation assays and to describe potential modifications to the procedure so that conditions can be optimized.

摘要

确定两种蛋白质是否能够相互作用最常用的方法之一是免疫共沉淀。免疫共沉淀依赖于抗体稳定且特异性结合包含诱饵蛋白的复合物的能力。该抗体提供了一种将这些复合物固定在固体基质上的方法,在本文介绍的实验方案中,这是通过与蛋白A相互作用来实现的,以便洗去无关蛋白。通过蛋白质印迹法来确定诱饵复合物中靶蛋白的存在。由于蛋白质 - 蛋白质相互作用的生化多样性,不可能描述适用于每个免疫沉淀实验的单一条件集。相反,本章的目的是为免疫共沉淀分析提供实际的起始条件,并描述该方法可能的改进,以便优化条件。

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