两步共免疫沉淀(TIP)

Q2 Biochemistry, Genetics and Molecular Biology Current Protocols in Molecular Biology Pub Date : 2018-10-30 DOI:10.1002/cpmb.80
Maria Rita Sciuto, Valeria Coppola, Gioacchin Iannolo, Ruggero De Maria, Tobias L. Haas
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引用次数: 2

摘要

在过去的几十年里,已经开发了许多方法来研究蛋白质-蛋白质和蛋白质-核酸相互作用(PPIs和PNIs)。亲和纯化方法如共免疫沉淀(co-IP)通常用于检测和分离由这些相互作用产生的大分子复合物。在本文中,我们描述了一种两步共免疫沉淀(TIP)技术。与标准co-IP相比,TIP在天然表达条件下分离PPIs或PNIs时提供了更高的特异性,显著减少了非特异性结合物的丰度,从而促进了相互作用复合物的下游分析。在这里,我们报告了一个详细的TIP程序,我们用它从伯基特淋巴瘤细胞和原代人CD4+ T细胞中纯化蛋白质-蛋白质复合物。此外,本单元还介绍了TIP在分离转录因子结合染色质方面的应用。©2018 by John Wiley &儿子,Inc。
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Two-Step Co-Immunoprecipitation (TIP)

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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Current Protocols in Molecular Biology
Current Protocols in Molecular Biology Biochemistry, Genetics and Molecular Biology-Molecular Biology
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