Identifying protein complexes via multi-network clustering

Ou-Yang Le, Hong Yan, Xiao-Fei Zhang
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引用次数: 1

Abstract

The detection of protein complexes from protein-protein interaction (PPI) networks is an important step toward understanding the functional organization within cells. A great number of graph clustering algorithms have been proposed to undertake this task. Since PPI data collected by high-throughput technologies is quite noisy, simply applying graph clustering algorithms on PPI data is generally not adequate to achieve reliable prediction results. Behind protein interactions, there are protein domains that interact with each other. Jointly exploiting protein-protein interactions and domain-domain interactions (DDI) have the potential to increase the accuracy of protein complex detection. However, traditional graph clustering algorithms focus on clustering proteins within a single PPI network, and cannot make use of information inherent in other heterogeneous networks. In this paper, we proposed a novel generative model to perform multi-network clustering. Unlike previous protein complex detection algorithms that can only utilize the information within a single PPI network, our model is a flexible framework that can take into account PPIs, DDIs and domain-protein associations to achieve more consistent and reliable clustering results. Experiment results on real data demonstrate that our method performs much better than state-of-the-art protein complex detection techniques.
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通过多网络聚类识别蛋白质复合物
从蛋白质-蛋白质相互作用(PPI)网络中检测蛋白质复合物是了解细胞内功能组织的重要一步。为了完成这一任务,已经提出了大量的图聚类算法。由于高通量技术采集的PPI数据具有较大的噪声,简单地对PPI数据应用图聚类算法通常不足以获得可靠的预测结果。在蛋白质相互作用的背后,有相互作用的蛋白质结构域。联合利用蛋白质-蛋白质相互作用和结构域-结构域相互作用(DDI)有可能提高蛋白质复合物检测的准确性。然而,传统的图聚类算法主要关注单个PPI网络中的蛋白质聚类,无法利用其他异构网络中固有的信息。本文提出了一种新的多网络聚类生成模型。与以往只能利用单个PPI网络中的信息的蛋白质复合物检测算法不同,我们的模型是一个灵活的框架,可以考虑PPI、ddi和结构域-蛋白质关联,以获得更一致和可靠的聚类结果。实际数据的实验结果表明,我们的方法比目前最先进的蛋白质复合物检测技术性能要好得多。
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