Detection of physical interactions by immunoprecipitation of FLAG- and HA-tagged proteins expressed at the his-3 locus in Neurospora crassa

Tsuyoshi Kawabata, H. Inoue
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引用次数: 16

Abstract

Protein function is often regulated through interactions with other protein(s) or by post-translational modifications. To understand these mechanisms, it is useful to utilize antibodies. However, it is not always certain whether a good antibody can be made for this purpose. The use of epitope tags eliminates the troubles associated with raising antibodies. In this report, we present a method to detect interactions between proteins by using two types of epitope-tagged proteins, FLAGand HA-tagged proteins in Neurospora. These constructs were introduced at and expressed from the his-3 locus in different strains. To examine protein-protein interactions, heterokaryons between these strains were constructed. We conclude that this strategy is a useful tool to investigate protein function and protein interactions.
粗神经孢子虫his-3位点表达的FLAG和ha标记蛋白的免疫沉淀检测物理相互作用
蛋白质的功能通常通过与其他蛋白质的相互作用或翻译后修饰来调节。为了理解这些机制,利用抗体是有用的。然而,是否可以为此目的制造出良好的抗体并不总是确定的。表位标签的使用消除了与提高抗体相关的麻烦。在这篇报道中,我们提出了一种检测蛋白之间相互作用的方法,通过两种类型的表位标记的蛋白,flaga和ha标记的蛋白在神经孢子虫。这些结构体在不同菌株的his-3位点被引入并表达。为了研究蛋白质之间的相互作用,构建了这些菌株之间的异核体。我们得出结论,该策略是研究蛋白质功能和蛋白质相互作用的有用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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