Disease-specific protein complex detection in the human protein interaction network with a supervised learning method

Ziwei Zhou, Yingyi Gui, Zhihao Yang, Xiaoxia Liu, Lei Wang, Yin Zhang, Hongfei Lin, Jian Wang
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引用次数: 3

Abstract

High-throughput experimental techniques have produced a large amount of human protein-protein interactions, making it possible to construct a large-scale human PPI network and detect human protein complexes from the network with computational approaches. However, most of current complex detection methods are based on graph theory which can't utilize the information of the known complexes. In this paper, we present a supervised learning method to detect protein complexes in a human PPI network. In this method, biological characteristics and properties of the network are taken into consideration to construct a rich feature set to train a regression model for protein complex detection. In addition, the specific disease related PPIs are extracted from biomedical literatures and then integrated into the original PPI network for detecting the disease-specific protein complexes more effectively. Experimental results show that the performance of our method is superior to other existing state-of-the-art methods. Furthermore, through the analysis of the breast cancer specific complexes detected with our method, more biological insights for breast cancer (e.g., some candidate susceptible genes of breast cancer) are provided.
人类蛋白质相互作用网络中疾病特异性蛋白质复合物检测的监督学习方法
高通量实验技术已经产生了大量的人类蛋白质-蛋白质相互作用,使得构建大规模的人类PPI网络和用计算方法从网络中检测人类蛋白质复合物成为可能。然而,目前的复合体检测方法大多是基于图论的,不能充分利用已知复合体的信息。在本文中,我们提出了一种监督学习方法来检测人体PPI网络中的蛋白质复合物。该方法综合考虑神经网络的生物学特性和网络特性,构建丰富的特征集,训练用于蛋白质复合体检测的回归模型。此外,从生物医学文献中提取与特定疾病相关的PPI,并将其整合到原始PPI网络中,以更有效地检测疾病特异性蛋白复合物。实验结果表明,该方法的性能优于现有的先进方法。此外,通过对我们的方法检测到的乳腺癌特异性复合物的分析,为乳腺癌提供了更多的生物学见解(如乳腺癌的一些候选易感基因)。
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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