Li Li, Zinovyeva Anna Y
Division of Biology, Kansas State University.
Division of Biology, Kansas State University;
J Vis Exp. 2020 May 23(159). doi: 10.3791/61243.
Co-immunoprecipitation methods are frequently used to study protein-protein interactions. Confirmation of hypothesized protein-protein interactions or identification of new ones can provide invaluable information about the function of a protein of interest. Some of the traditional methods for extract preparation frequently require labor-intensive and time-consuming techniques. Here, a modified extract preparation protocol using a bead mill homogenizer and metal beads is described as a rapid alternative to traditional protein preparation methods. This extract preparation method is compatible with downstream co-immunoprecipitation studies. As an example, the method was used to successfully co-immunoprecipitate C. elegans microRNA Argonaute ALG-1 and two known ALG-1 interactors: AIN-1, and HRPK-1. This protocol includes descriptions of animal sample collection, extract preparation, extract clarification, and protein immunoprecipitation. The described protocol can be adapted to test for interactions between any two or more endogenous, endogenously tagged, or overexpressed C. elegans proteins in a variety of genetic backgrounds.
免疫共沉淀方法常用于研究蛋白质-蛋白质相互作用。对假设的蛋白质-蛋白质相互作用进行确认或鉴定新的相互作用,可为感兴趣的蛋白质功能提供宝贵信息。一些传统的提取物制备方法通常需要耗费大量人力和时间的技术。在此,描述了一种使用珠磨匀浆器和金属珠的改良提取物制备方案,作为传统蛋白质制备方法的快速替代方法。这种提取物制备方法与下游免疫共沉淀研究兼容。例如,该方法成功用于免疫共沉淀秀丽隐杆线虫微小RNA Argonaute ALG-1以及两个已知的ALG-1相互作用蛋白:AIN-1和HRPK-1。该方案包括动物样本采集、提取物制备、提取物澄清和蛋白质免疫沉淀的描述。所描述的方案可适用于在多种遗传背景下测试任意两种或更多种内源性、内源性标记或过表达的秀丽隐杆线虫蛋白质之间的相互作用。