免疫沉淀
染色质免疫沉淀
核酸
化学
计算生物学
高分子
分子生物学
转录因子
邻近连接试验
细胞生物学
生物
生物化学
基因表达
基因
发起人
受体
作者
Maria Rita Sciuto,Valeria Coppola,Gioacchin Iannolo,Ruggero De Maria,Tobias L. Haas
摘要
Abstract In the past few decades, numerous approaches have been developed to investigate protein‐protein and protein‐nucleic acid interactions (PPIs and PNIs). Affinity purification methods such as co‐immunoprecipitation (co‐IP) are commonly used to detect and isolate the macromolecular complexesresulting from these interactions. In this article, we describe a two‐step co‐immunoprecipitation (TIP) technique. As compared to standard co‐IP, TIP provides increased specificity in the isolation of PPIs or PNIs under native expression conditions, dramatically reducing the abundance of nonspecific binders and thus facilitating downstream analyses of the interaction complexes. Here, we report a detailed TIP procedure that we used to purify a protein‐protein complex from Burkitt lymphoma cells and from primary human CD4 + T cells. In addition, this unit describes an application of TIP for the isolation of transcription‐factor‐bound chromatin. © 2018 by John Wiley & Sons, Inc.
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