Centrality Measure Analysis on Protein Interaction Networks

Anooja Ali, Vishwanath R. Hulipalled, S. Patil
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引用次数: 4

Abstract

Analysis of protein interaction is widely recognized to understand cell physiology and disease conditions. The increase in the accumulation of these interaction data facilitates the recognition of the essential proteins in Protein Protein Interaction (PPI) networks. An array of centrality measures are available to uncover essential proteins in PPI networks. However, majority approaches are centered around topological properties of PPI. Few approaches integrate gene annotation with topology for predicting essential proteins. This biological framework in PPI network are inferred in terms of graph-theoretic approaches. The topological analysis focuses on protein, their interactions, and the subnetworks. In this research, we review the common centrality measures. We thoroughly studied the centrality aspect of each node in the PPI to detect the influential nodes and the impact of topological features in centrality measures. We applied centrality measures to the PPI networks obtained from the Biological General Repository for Interaction Networks (BioGRID) and Mammalian Protein Protein Database (MIPS) datasets. The experimental evaluation shows the behavior of centrality measures to the datasets.
蛋白质相互作用网络的中心性测度分析
蛋白质相互作用的分析被广泛认为是了解细胞生理和疾病状况的重要手段。这些相互作用数据积累的增加促进了蛋白质相互作用(PPI)网络中必需蛋白质的识别。一系列中心性措施可用于发现PPI网络中的必需蛋白质。然而,大多数方法都是围绕PPI的拓扑性质。很少有方法将基因注释与拓扑学结合起来预测必需蛋白质。这种生物框架在PPI网络是推断在图论的方法。拓扑分析的重点是蛋白质、它们之间的相互作用和子网。在本研究中,我们回顾了常见的中心性度量。我们深入研究了PPI中每个节点的中心性方面,以检测有影响的节点和拓扑特征对中心性度量的影响。我们对从相互作用网络生物总库(BioGRID)和哺乳动物蛋白质数据库(MIPS)数据集中获得的PPI网络应用了中心性度量。实验评估显示了中心性度量对数据集的行为。
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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