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Identification of essential proteins from weighted protein-protein interaction networks (Conference Paper)

机译:从加权蛋白质-蛋白质相互作用网络中鉴定必需蛋白质(会议论文)

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摘要

Identifying essential proteins is very important for understanding the minimal requirements of cellular survival and development. Fast growth in the amount of available protein-protein interactions has produced unprecedented opportunities for detecting protein essentiality on network level. A series of centrality measures have been proposed to discover essential proteins based on network topology. Unfortunately, the protein-protein interactions produced by high-throughput experiments generally have high false positives. Moreover, most of centrality measures based on network topology are sensitive to false positives. We therefore propose a new method for evaluating the confidence of each interaction based on the combination of logistic regression-based model and function similarity. Nine standard centrality measures in weighted network were redefined in this paper. The experimental results on a yeast protein interaction network shows that the weighting method improved the performance of centrality measures considerably. More essential proteins were discovered by the weighted centrality measures than by the original centrality measures used in the unweighted network. Even about 20% improvements were obtained from closeness centrality and subgraph centrality.
机译:鉴定必需蛋白质对于理解细胞存活和发育的最低要求非常重要。可用蛋白质-蛋白质相互作用量的快速增长为检测网络一级的蛋白质必需性提供了前所未有的机会。已经提出了一系列集中性措施来发现基于网络拓扑的必需蛋白质。不幸的是,由高通量实验产生的蛋白质-蛋白质相互作用通常具有较高的假阳性。此外,大多数基于网络拓扑的集中度度量都对误报敏感。因此,我们提出了一种新的方法,用于基于逻辑回归模型和功能相似性的组合来评估每个交互的置信度。本文重新定义了加权网络中的九种标准集中度度量。酵母蛋白质相互作用网络上的实验结果表明,加权方法大大提高了集中度测量的性能。通过加权中心度度量比在未加权网络中使用的原始中心度度量发现了更多的必需蛋白质。从紧密度中心度和子图中心度甚至可以获得约20%的改进。

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