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首页> 外文期刊>BMC Genomics >High-throughput mammalian two-hybrid screening for protein-protein interactions using transfected cell arrays
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High-throughput mammalian two-hybrid screening for protein-protein interactions using transfected cell arrays

机译:使用转染的细胞阵列对蛋白质相互作用进行高通量哺乳动物二杂交筛选

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Background Most of the biological processes rely on the formation of protein complexes. Investigation of protein-protein interactions (PPI) is therefore essential for understanding of cellular functions. It is advantageous to perform mammalian PPI analysis in mammalian cells because the expressed proteins can then be subjected to essential post-translational modifications. Until now mammalian two-hybrid assays have been performed on individual gene scale. We here describe a new and cost-effective method for the high-throughput detection of protein-protein interactions in mammalian cells that combines the advantages of mammalian two-hybrid systems with those of DNA microarrays. Results In this cell array protein-protein interaction assay (CAPPIA), mixtures of bait and prey expression plasmids together with an auto-fluorescent reporter are immobilized on glass slides in defined array formats. Adherent cells that grow on top of the micro-array will become fluorescent only if the expressed proteins interact and subsequently trans-activate the reporter. Using known interaction partners and by screening 160 different combinations of prey and bait proteins associated with the human androgen receptor we demonstrate that this assay allows the quantitative detection of specific protein interactions in different types of mammalian cells and under the influence of different compounds. Moreover, different strategies in respect to bait-prey combinations are presented. Conclusion We demonstrate that the CAPPIA assay allows the quantitative detection of specific protein interactions in different types of mammalian cells and under the influence of different compounds. The high number of preys that can be tested per slide together with the flexibility to interrogate any bait of interest and the small amounts of reagents that are required makes this assay currently one of the most economical high-throughput detection assays for protein-protein interactions in mammalian cells.
机译:背景技术大多数生物学过程都依赖于蛋白质复合物的形成。因此,蛋白质-蛋白质相互作用(PPI)的研究对于理解细胞功能至关重要。在哺乳动物细胞中进行哺乳动物PPI分析是有利的,因为随后可以对表达的蛋白质进行必要的翻译后修饰。迄今为止,已经在单个基因规模上进行了哺乳动物两杂交试验。我们在这里描述了一种新的且具有成本效益的方法,用于高通量检测哺乳动物细胞中的蛋白质-蛋白质相互作用,结合了哺乳动物双杂交系统与DNA微阵列的优势。结果在该细胞阵列蛋白-蛋白质相互作用测定法(CAPPIA)中,诱饵和猎物表达质粒的混合物以及自发荧光报道分子以固定的阵列形式固定在载玻片上。仅在表达的蛋白质相互作用并随后反激活报道分子的情况下,在微阵列顶部生长的粘附细胞才会发荧光。使用已知的相互作用伙伴并通过筛选160种与人类雄激素受体相关的猎物和诱饵蛋白的不同组合,我们证明了该测定方法可以定量检测不同类型的哺乳动物细胞中以及在不同化合物的影响下特定蛋白相互作用。此外,提出了关于诱饵-猎物组合的不同策略。结论我们证明了CAPPIA测定法可以定量检测不同类型的哺乳动物细胞中以及在不同化合物的影响下特异性蛋白质相互作用。每个载玻片上可以测试的猎物数量众多,并且可以讯问任何诱饵,并且所需试剂数量少,因此这种测定法目前是最经济的蛋白质-蛋白质相互作用高通量检测测定法之一。哺乳动物细胞。

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