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Improving protein complex prediction by reconstructing a high-confidence protein-protein interaction network of Escherichia coli from different physical interaction data sources

机译:通过从不同的物理相互作用数据源重构大肠杆菌的高可信蛋白-蛋白相互作用网络来改善蛋白复合物的预测

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Background Although different protein-protein physical interaction (PPI) datasets exist for Escherichia coli , no common methodology exists to integrate these datasets and extract reliable modules reflecting the existing biological process and protein complexes. Na?ve Bayesian formula is the highly accepted method to integrate different PPI datasets into a single weighted PPI network, but detecting proper weights in such network is still a major problem. Results In this paper, we proposed a new methodology to integrate various physical PPI datasets into a single weighted PPI network in a way that the detected modules in PPI network exhibit the highest similarity to available functional modules. We used the co-expression modules as functional modules, and we shown that direct functional modules detected from Gene Ontology terms could be used as an alternative dataset. After running this integrating methodology over six different physical PPI datasets, orthologous high-confidence interactions from a related organism and two AP-MS PPI datasets gained high weights in the integrated networks, while the weights for one AP-MS PPI dataset and two other datasets derived from public databases have converged to zero. The majority of detected modules shaped around one or few hub protein(s). Still, a large number of highly interacting protein modules were detected which are functionally relevant and are likely to construct protein complexes. Conclusions We provided a new high confidence protein complex prediction method supported by functional studies and literature mining.
机译:背景技术尽管针对大肠杆菌存在不同的蛋白质-蛋白质物理相互作用(PPI)数据集,但不存在通用方法来整合这些数据集并提取反映现有生物过程和蛋白质复合物的可靠模块。朴素贝叶斯公式是将不同的PPI数据集集成到单个加权PPI网络中的一种广为接受的方法,但是在这种网络中检测适当的权重仍然是一个主要问题。结果在本文中,我们提出了一种新的方法,可以将各种物理PPI数据集集成到单个加权PPI网络中,以使PPI网络中检测到的模块与可用功能模块的相似性最高。我们将共表达模块用作功能模块,并且我们表明从基因本体论术语中检测到的直接功能模块可以用作备用数据集。在六个不同的物理PPI数据集上运行此集成方法后,相关生物与两个AP-MS PPI数据集的直系同源高可信度交互在集成网络中获得了较高的权重,而一个AP-MS PPI数据集和其他两个数据集的权重从公共数据库派生的数据已收敛到零。大部分检测到的模块围绕一种或几种毂蛋白形成。尽管如此,仍检测到大量高度相互作用的蛋白质模块,它们在功能上相关并且很可能构建蛋白质复合物。结论我们提供了一种新的高可信度蛋白质复合物预测方法,该方法得到了功能研究和文献挖掘的支持。

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