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Network-based analysis of reverse phase protein array data

机译:基于网络的反相蛋白质阵列数据分析

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In this paper, we introduce a computational method for constructing networks based on reverse phase protein array (RPPA) data to identify complex patterns in protein signaling. The method is applied to phosphoproteomic profiles of basal expression and activation/phosphorylation of 76 key signaling proteins in three breast cancer cell lines (MCF7, LCC1, and LCC9). Temporal RPPA data are acquired at 48h, 96h, and 144h after knocking down four genes in separate experiments. These genes are selected from a previous study as important determinants for breast cancer survival. Interaction networks between the proteins and phosphorylated proteins are constructed by analyzing the expression levels of protein pairs using a multivariate analysis of variance model. A new scoring criterion is introduced to determine the proteins that changed significantly at each of the three time points. Signaling networks are constructed based on statistically significant protein pairs selected from the RPPA data. Through a topology based analysis, we search for wiring patterns to help identify key network nodes that are associated with protein expression changes in various experimental conditions.
机译:在本文中,我们介绍了一种基于反相蛋白质阵列(RPPA)数据构建网络的计算方法,以识别蛋白质信号中的复杂模式。该方法适用于三种乳腺癌细胞系(MCF7,LCC1和LCC9)的基础表达和76种关键信号蛋白的激活/磷酸化的磷酸化蛋白质组学分析。在单独的实验中敲除四个基因后的48h,96h和144h采集了时间RPPA数据。这些基因选自先前的研究,作为乳腺癌生存的重要决定因素。通过使用方差模型的多变量分析来分析蛋白质对的表达水平,可以构建蛋白质与磷酸化蛋白质之间的相互作用网络。引入了新的评分标准,以确定在三个时间点的每个时间点发生显着变化的蛋白质。信号网络是基于从RPPA数据中选择的具有统计学意义的蛋白质对构建的。通过基于拓扑的分析,我们搜索接线方式,以帮助识别与各种实验条件下蛋白质表达变化相关的关键网络节点。

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