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Uncover protein complexes in E.coli network

机译:在大肠杆菌网络中发现蛋白质复合物

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Recent advances in proteomic technologies have enabled high-throughput binary data on protein-protein interactions of E. coli to be released into public domain, and many protein complexes have been identified by experimental methods. Although it has a long study history, a large-scale analysis of protein complex in binary PPI network of E. coli is still absent. We used a novel link clustering algorithm named ELPA to infer protein complexes and functional modules in E. coli PPI network. By mapping our results to 276 gold standard protein complexes and protein function annotations offered by EcoCyc, we found that 80.2% of predicted modules mapping well with one or more complexes, while 92.8% of predicted modules tally well with certain GO terms. Furthermore, we compare our results with MCL algorithm, and evaluated our results with several accuracy measures and biological relevance, the result shows that ELPA achieved an average 18.3% improvement over MCL based on the accuracy measures, which means our method will contributes to uncover the complexes of Ecoli.
机译:蛋白质组学技术的最新进展已使有关大肠杆菌蛋白质-蛋白质相互作用的高通量二进制数据得以发布到公共领域,并且许多蛋白质复合物已通过实验方法得到鉴定。尽管已有很长的研究历史,但仍缺乏对大肠杆菌二元PPI网络中蛋白质复合物的大规模分析。我们使用一种名为ELPA的新型链接聚类算法来推断E. coli PPI网络中的蛋白质复合物和功能模块。通过将我们的结果映射到EcoCyc提供的276个金标准蛋白质复合物和蛋白质功能注释,我们发现80.2%的预测模块与一种或多种复合物的对应关系很好,而92.8%的预测模块与某些GO术语的吻合很好。此外,我们将我们的结果与MCL算法进行比较,并通过几种准确性度量和生物学相关性评估了我们的结果,结果表明,基于准确性度量,ELPA比MCL平均提高了18.3%,这意味着我们的方法将有助于发现Ecoli的配合物。

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