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Network-assisted protein identification and data interpretation in shotgun proteomics

机译:shot弹枪蛋白质组学中的网络辅助蛋白质鉴定和数据解释

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摘要

Protein assembly and biological interpretation of the assembled protein lists are critical steps in shotgun proteomics data analysis. Although most biological functions arise from interactions among proteins, current protein assembly pipelines treat proteins as independent entities. Usually, only individual proteins with strong experimental evidence, that is, confident proteins, are reported, whereas many possible proteins of biological interest are eliminated. We have developed a clique-enrichment approach (CEA) to rescue eliminated proteins by incorporating the relationship among proteins as embedded in a protein interaction network. In several data sets tested, CEA increased protein identification by 8–23% with an estimated accuracy of 85%. Rescued proteins were supported by existing literature or transcriptome profiling studies at similar levels as confident proteins and at a significantly higher level than abandoned ones. Applying CEA on a breast cancer data set, rescued proteins coded by well-known breast cancer genes. In addition, CEA generated a network view of the proteins and helped show the modular organization of proteins that may underpin the molecular mechanisms of the disease.
机译:蛋白质组装和组装蛋白质列表的生物学解释是shot弹枪蛋白质组学数据分析中的关键步骤。尽管大多数生物学功能是由蛋白质之间的相互作用产生的,但是当前的蛋白质组装管道将蛋白质视为独立的实体。通常,仅报告具有强大实验证据的单个蛋白质,即可信蛋白质,而许多具有生物学意义的可能蛋白质则被消除。我们已经开发了一种集团浓缩方法(CEA),通过整合嵌入蛋白质相互作用网络中的蛋白质之间的关系来挽救消除的蛋白质。在多个测试数据集中,CEA使蛋白质鉴定提高了8–23%,估计准确性为85%。现有文献或转录组谱分析研究支持被拯救的蛋白质,其水平与可信蛋白质相似,并且比被丢弃的蛋白质高得多。将CEA应用于乳腺癌数据集,可以拯救由知名乳腺癌基因编码的蛋白质。此外,CEA生成了蛋白质的网络视图,并帮助显示了可能支撑疾病分子机制的蛋白质模块化组织。

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