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A rapid and accurate approach for prediction of interactomes from co-elution data (PrInCE)

机译:从共洗脱数据(PrInCE)预测相互作用组的快速准确方法

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An organism’s protein interactome, or complete network of protein-protein interactions, defines the protein complexes that drive cellular processes. Techniques for studying protein complexes have traditionally applied targeted strategies such as yeast two-hybrid or affinity purification-mass spectrometry to assess protein interactions. However, given the vast number of protein complexes, more scalable methods are necessary to accelerate interaction discovery and to construct whole interactomes. We recently developed a complementary technique based on the use of protein correlation profiling (PCP) and stable isotope labeling in amino acids in cell culture (SILAC) to assess chromatographic co-elution as evidence of interacting proteins. Importantly, PCP-SILAC is also capable of measuring protein interactions simultaneously under multiple biological conditions, allowing the detection of treatment-specific changes to an interactome. Given the uniqueness and high dimensionality of co-elution data, new tools are needed to compare protein elution profiles, control false discovery rates, and construct an accurate interactome. Here we describe a freely available bioinformatics pipeline, PrInCE, for the analysis of co-elution data. PrInCE is a modular, open-source library that is computationally inexpensive, able to use label and label-free data, and capable of detecting tens of thousands of protein-protein interactions. Using a machine learning approach, PrInCE offers greatly reduced run time, more predicted interactions at the same stringency, prediction of protein complexes, and greater ease of use over previous bioinformatics tools for co-elution data. PrInCE is implemented in Matlab (version R2017a). Source code and standalone executable programs for Windows and Mac OSX are available at https://github.com/fosterlab/PrInCE , where usage instructions can be found. An example dataset and output are also provided for testing purposes. PrInCE is the first fast and easy-to-use data analysis pipeline that predicts interactomes and protein complexes from co-elution data. PrInCE allows researchers without bioinformatics expertise to analyze high-throughput co-elution datasets.
机译:生物体的蛋白质相互作用组或蛋白质-蛋白质相互作用的完整网络定义了驱动细胞过程的蛋白质复合物。传统上,研究蛋白质复合物的技术采用靶向策略,例如酵母双杂交或亲和纯化-质谱法来评估蛋白质相互作用。但是,鉴于蛋白质复合物的数量众多,需要更多可扩展的方法来加快相互作用的发现并构建整个相互作用组。我们最近开发了一种互补技术,该技术基于蛋白相关分析(PCP)和细胞培养氨基酸(SILAC)中氨基酸的稳定同位素标记来评估色谱共洗脱作为相互作用蛋白的证据。重要的是,PCP-SILAC还能够同时在多种生物学条件下测量蛋白质相互作用,从而能够检测相互作用组的治疗特异性变化。鉴于共洗脱数据的独特性和高维性,需要新的工具来比较蛋白质洗脱谱,控制错误发现率并构建准确的相互作用组。在这里,我们描述了免费的生物信息学管道PrInCE,用于分析共洗脱数据。 PrInCE是一个模块化的开放源代码库,在计算上不昂贵,能够使用标签和无标签数据,并且能够检测成千上万的蛋白质-蛋白质相互作用。与以前的生物信息学工具相比,PrInCE使用机器学习方法,大大减少了运行时间,在相同的严格性下预测了更多的相互作用,预测了蛋白质复合物,并且更易于使用共洗脱数据。 PrInCE在Matlab(版本R2017a)中实现。可在https://github.com/fosterlab/PrInCE上找到Windows和Mac OSX的源代码和独立的可执行程序,可以在其中找到使用说明。还提供了示例数据集和输出以用于测试目的。 PrInCE是第一个快速且易于使用的数据分析管道,可根据共洗脱数据预测相互作用基因组和蛋白质复合物。 PrInCE允许没有生物信息学专业知识的研究人员分析高通量共洗脱数据集。

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