Takahashi Yoshinori
Department of Pediatrics, The Pennsylvania State University College of Medicine, 500 University Drive, Hershey, PA, 17033, USA,
Methods Mol Biol. 2015;1278:381-9. doi: 10.1007/978-1-4939-2425-7_25.
Co-immunoprecipitation (Co-IP) is one of the most widely used methods to identify novel proteins that associate with a protein of interest or to determine complex formation between known proteins. For this technique, a protein of interest is captured using a specific antibody. The antibody-bound protein, as well as any proteins bound to the protein of interest, is then precipitated using a resin (immunoprecipitation, IP). Proteins that are not bound to the protein of interest are then removed from the sample with a series of washes. The resulting immunocomplexes are then analyzed by immunoblot. As the requirements for protein-protein interactions vary, optimal experimental conditions for examining the interacting partners of different proteins of interest must be determined empirically. Once appropriate experimental conditions have been established, the IP/Co-IP procedure is simple and straightforward. In this chapter, a standard protocol for IP/co-IP, with several key factors for the success of IP/co-IP analyses, is discussed.
免疫共沉淀(Co-IP)是用于鉴定与目标蛋白相互作用的新蛋白或确定已知蛋白之间复合物形成的最广泛使用的方法之一。对于该技术,使用特异性抗体捕获目标蛋白。然后使用树脂沉淀与抗体结合的蛋白以及与目标蛋白结合的任何蛋白(免疫沉淀,IP)。接着通过一系列洗涤从样品中去除未与目标蛋白结合的蛋白。然后通过免疫印迹分析所得的免疫复合物。由于蛋白质-蛋白质相互作用的要求各不相同,必须根据经验确定用于检测不同目标蛋白相互作用伙伴的最佳实验条件。一旦建立了合适的实验条件,IP/Co-IP程序就简单明了。在本章中,将讨论IP/co-IP的标准方案以及IP/co-IP分析成功的几个关键因素。