Discovering essential proteins based on PPI network and protein complex.

Pub Date : 2015-01-01 DOI:10.1504/ijdmb.2015.068951
Jun Ren, Jianxin Wang, Min Li, Fangxiang Wu
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引用次数: 25

Abstract

Most computational methods for identifying essential proteins focus on the topological centrality of protein-protein interaction (PPI) networks. However, these methods have limitations, such as the difficulty for identifying essential proteins with low centrality values and the poor performance for incomplete PPI network. In this paper, protein complex is proven to be an important factor for determining protein essentiality and a new centrality measure, complex centrality, is proposed. The weighted average of complex centrality and subgraph centrality, called harmonic centrality (HC), is proposed to predict essential proteins. It combines PPI network topology and protein complex information and has better performance than methods based on PPI network. The improvement is higher when the PPI network is incomplete. Furthermore, a weighted PPI network is generated by integrating cellular localisation and biological process to a PPI network. The performance of HC measure is improved 5% in this weighted PPI network.

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基于PPI网络和蛋白质复合物发现必需蛋白质。
大多数识别必需蛋白质的计算方法都集中在蛋白质-蛋白质相互作用(PPI)网络的拓扑中心性上。然而,这些方法存在局限性,例如难以识别具有低中心性值的必需蛋白质,以及不完整PPI网络的性能较差。本文证明了蛋白质复合体是决定蛋白质本质的重要因素,并提出了一种新的中心性度量方法——复合体中心性。提出了复杂中心性和子图中心性的加权平均值,称为调和中心性(HC),用于预测必需蛋白质。该方法结合了PPI网络拓扑结构和蛋白质复合物信息,比基于PPI网络的方法具有更好的性能。当PPI网络不完整时,改善程度更高。此外,通过将细胞定位和生物过程整合到PPI网络中,生成加权PPI网络。在该加权PPI网络中,HC测度的性能提高了5%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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