Detection of protein complex from protein-protein interaction network using Markov clustering

P. Ochieng, W. Kusuma, Toto Haryanto
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引用次数: 14

Abstract

Detection of complexes, or groups of functionally related proteins, is an important challenge while analysing biological networks. However, existing algorithms to identify protein complexes are insufficient when applied to dense networks of experimentally derived interaction data. Therefore, we introduced a graph clustering method based on Markov clustering algorithm to identify protein complex within highly interconnected protein-protein interaction networks. Protein-protein interaction network was first constructed to develop geometrical network, the network was then partitioned using Markov clustering to detect protein complexes. The interest of the proposed method was illustrated by its application to Human Proteins associated to type II diabetes mellitus. Flow simulation of MCL algorithm was initially performed and topological properties of the resultant network were analysed for detection of the protein complex. The results indicated the proposed method successfully detect an overall of 34 complexes with 11 complexes consisting of overlapping modules and 20 non-overlapping modules. The major complex consisted of 102 proteins and 521 interactions with cluster modularity and density of 0.745 and 0.101 respectively. The comparison analysis revealed MCL out perform AP, MCODE and SCPS algorithms with high clustering coefficient (0.751) network density and modularity index (0.630). This demonstrated MCL was the most reliable and efficient graph clustering algorithm for detection of protein complexes from PPI networks.
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利用马尔可夫聚类从蛋白-蛋白相互作用网络中检测蛋白复合体
在分析生物网络时,检测复合物或功能相关蛋白群是一个重要的挑战。然而,现有的识别蛋白质复合物的算法在应用于实验导出的相互作用数据的密集网络时是不够的。因此,我们引入了一种基于马尔可夫聚类算法的图聚类方法来识别高度互连的蛋白质-蛋白质相互作用网络中的蛋白质复合物。首先构建蛋白质-蛋白质相互作用网络,形成几何网络,然后利用马尔可夫聚类对网络进行分割,检测蛋白质复合物。提出的方法的兴趣是由其应用于人类蛋白相关的II型糖尿病。首先进行了MCL算法的流动模拟,并分析了所得网络的拓扑特性,以检测蛋白质复合物。结果表明,该方法共检测出34个配合物,其中11个为重叠模块,20个为非重叠模块。主要复合物由102个蛋白和521个相互作用组成,簇的模量和密度分别为0.745和0.101。对比分析表明,MCL算法具有较高的聚类系数(0.751)、网络密度和模块化指数(0.630),优于AP、MCODE和SCPS算法。这表明MCL是最可靠和有效的图聚类算法,用于检测来自PPI网络的蛋白质复合物。
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