Identifying Protein Complexes Method Based on Time-Sequenced Association and Ant Colony Clustering in Dynamic PPI Networks

Cuicui Yang, Junzhong Ji, Jia Wei Lv
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引用次数: 1

Abstract

As protein-protein interactions always change with time, environments and different stages of cell cycle, the clustering analysis on static protein-protein interaction (PPI) networks can not reflect this dynamics property and is far from satisfactory. To solve it, this paper proposes a method based on time-sequenced association and Ant Colony Clustering for identifying Protein Complexes in Dynamic PPI networks (called ACC-DPC). ACC-DPC first splits a PPI network into a series of dynamics subnetworks under different time points by integrating gene expression data, and then makes the clustering analysis on each subnetwork using the ant colony clustering method. For each subnetwork, ACC-DPC begins with constructing initial protein clusters by introducing the time-sequenced association characteristic of protein complexes between two adjacent time points, and later uses the picking up and dropping down operators of ant colony clustering to accomplish the clustering process of other proteins. The experimental results on two PPI datasets demonstrate that ACC-DPC has competitive performances in identifying protein complexes of dynamic PPI networks compared with several algorithms.
动态PPI网络中基于时间序列关联和蚁群聚类的蛋白质复合物识别方法
由于蛋白质-蛋白质相互作用总是随着时间、环境和细胞周期的不同阶段而变化,静态蛋白质-蛋白质相互作用(PPI)网络的聚类分析不能反映这种动态特性,远远不能令人满意。为了解决这一问题,本文提出了一种基于时间序列关联和蚁群聚类的动态PPI网络蛋白复合物识别方法(ACC-DPC)。ACC-DPC首先通过整合基因表达数据,将PPI网络在不同时间点下划分为一系列动态子网络,然后利用蚁群聚类方法对每个子网络进行聚类分析。对于每个子网络,ACC-DPC首先通过引入相邻两个时间点之间蛋白质复合物的时间序列关联特征构建初始蛋白质簇,然后使用蚁群聚类的拾取和下降算子完成其他蛋白质的聚类过程。在两个PPI数据集上的实验结果表明,与几种算法相比,ACC-DPC在识别动态PPI网络的蛋白质复合物方面具有竞争力。
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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