Zhang Wei, Zou Xiufen
IEEE/ACM Trans Comput Biol Bioinform. 2015 Jul-Aug;12(4):879-86. doi: 10.1109/TCBB.2014.2386314.
The identification of protein complexes in protein-protein interaction (PPI) networks is fundamental for understanding biological processes and cellular molecular mechanisms. Many graph computational algorithms have been proposed to identify protein complexes from PPI networks by detecting densely connected groups of proteins. These algorithms assess the density of subgraphs through evaluation of the sum of individual edges or nodes; thus, incomplete and inaccurate measures may miss meaningful biological protein complexes with functional significance. In this study, we propose a novel method for assessing the compactness of local subnetworks by measuring the number of three node cliques. The present method detects each optimal cluster by growing a seed and maximizing the compactness function. To demonstrate the efficacy of the new proposed method, we evaluate its performance using five PPI networks on three reference sets of yeast protein complexes with five different measurements and compare the performance of the proposed method with four state-of-the-art methods. The results show that the protein complexes generated by the proposed method are of better quality than those generated by four classic methods. Therefore, the new proposed method is effective and useful for detecting protein complexes in PPI networks.
在蛋白质-蛋白质相互作用(PPI)网络中识别蛋白质复合物对于理解生物过程和细胞分子机制至关重要。已经提出了许多图计算算法,通过检测紧密连接的蛋白质组来从PPI网络中识别蛋白质复合物。这些算法通过评估单个边或节点的总和来评估子图的密度;因此,不完整和不准确的度量可能会遗漏具有功能意义的有意义的生物蛋白质复合物。在本研究中,我们提出了一种通过测量三节点团的数量来评估局部子网紧凑性的新方法。本方法通过生长种子并最大化紧凑性函数来检测每个最优簇。为了证明新提出方法的有效性,我们使用五个PPI网络在酵母蛋白质复合物的三个参考集上用五种不同的度量评估其性能,并将所提出方法的性能与四种最先进的方法进行比较。结果表明,所提出方法生成的蛋白质复合物质量优于四种经典方法生成的蛋白质复合物。因此,新提出的方法对于检测PPI网络中的蛋白质复合物是有效且有用的。