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A Topology Potential-Based Method for Identifying Essential Proteins from PPI Networks

机译:基于拓扑势的PPI网络识别必需蛋白的方法

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Essential proteins are indispensable for cellular life. It is of great significance to identify essential proteins that can help us understand the minimal requirements for cellular life and is also very important for drug design. However, identification of essential proteins based on experimental approaches are typically time-consuming and expensive. With the development of high-throughput technology in the post-genomic era, more and more protein-protein interaction data can be obtained, which make it possible to study essential proteins from the network level. There have been a series of computational approaches proposed for predicting essential proteins based on network topologies. Most of these topology based essential protein discovery methods were to use network centralities. In this paper, we investigate the essential proteins’ topological characters from a completely new perspective. To our knowledge it is the first time that topology potential is used to identify essential proteins from a protein-protein interaction (PPI) network. The basic idea is that each protein in the network can be viewed as a material particle which creates a potential field around itself and the interaction of all proteins forms a topological field over the network. By defining and computing the value of each protein’s topology potential, we can obtain a more precise ranking which reflects the importance of proteins from the PPI network. The experimental results show that topology potential-based methods TP and TP-NC outperform traditional topology measures: degree centrality (DC), betweenness centrality (BC), closeness centrality (CC), subgraph centrality (SC), eigenvector centrality (EC), information centrality (IC), and network centrality (NC) for predicting essential proteins. In addition, these centrality measures are improved on their performance for identifying essential proteins in biological network when controlled by topology potential.
机译:必需蛋白对于细胞生命是必不可少的。鉴定出可以帮助我们了解细胞生命的最低要求的必需蛋白质,对药物设计也非常重要。然而,基于实验方法鉴定必需蛋白质通常是耗时且昂贵的。随着后基因组时代高通量技术的发展,可以获得越来越多的蛋白质-蛋白质相互作用数据,这使得从网络层面研究必需蛋白质成为可能。已经提出了一系列用于基于网络拓扑结构预测必需蛋白质的计算方法。这些基于拓扑的基本蛋白质发现方法大多数都使用网络中心。在本文中,我们将从一个全新的角度研究必需蛋白质的拓扑特征。据我们所知,这是首次利用拓扑潜力从蛋白质-蛋白质相互作用(PPI)网络中识别必需蛋白质。基本思想是,网络中的每种蛋白质都可以看作是一种物质粒子,可以在其周围创建一个势场,并且所有蛋白质的相互作用都可以在网络上形成拓扑场。通过定义和计算每种蛋白质拓扑潜力的价值,我们可以获得更精确的排名,反映了PPI网络中蛋白质的重要​​性。实验结果表明,基于拓扑势的方法TP和TP-NC优于传统的拓扑度量:度中心(DC),中间中心(BC),紧密中心(CC),子图中心(SC),特征向量中心(EC),信息中心(IC)和网络中心(NC)来预测必需蛋白质。此外,这些集中度度量在通过拓扑势控制时在识别生物网络中必需蛋白质的性能上得到了改进。

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