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Temporal Protein Complex Identification Based on Dynamic Heterogeneous Protein Information Network Representation Learning

计算机科学 生物网络 代表(政治) 鉴定(生物学) 语义学(计算机科学) 异构网络 人工智能 一致性(知识库) 理论计算机科学 机器学习 数据挖掘 计算生物学 生物 政治学 无线网络 政治 程序设计语言 法学 无线 植物 电信
作者
Zeqian Li,Yijia Zhang,Peixuan Zhou
出处
期刊:IEEE/ACM Transactions on Computational Biology and Bioinformatics [Institute of Electrical and Electronics Engineers]
卷期号:21 (5): 1-11 被引量:2
标识
DOI:10.1109/tcbb.2024.3351078
摘要

Protein complexes, as the fundamental units of cellular function and regulation, play a crucial role in understanding the normal physiological functions of cells. Existing methods for protein complex identification attempt to introduce other biological information on top of the protein-protein interaction (PPI) network to assist in evaluating the degree of association between proteins. However, these methods usually treat protein interaction networks as flat homogeneous static networks. They cannot distinguish the roles and importance of different types of biological information, nor can they reflect the dynamic changes of protein complexes. In recent years, heterogeneous network representation learning has achieved great success in processing complex heterogeneous information and mining deep semantics. We thus propose a temporal protein complex identification method based on Dynamic Heterogeneous Protein information network Representation Learning, DHPRL. DHPRL naturally integrates multiple types of heterogeneous biological information in the cellular temporal dimension. It simultaneously models the temporal dynamic properties of proteins and the heterogeneity of biological information to improve the understanding of protein interactions and the accuracy of complex prediction. Firstly, we construct Dynamic Heterogeneous Protein Information Network (DHPIN) by integrating temporal gene expression information and GO attribute information. Then we design a dual-view collaborative contrast mechanism. Specifically, proposing to learn protein representations from two views of DHPIN (1-hop relation view and meta-path view) to model the consistency and specificity between nearest-neighbour bio information and deeper biological semantics. The dynamic PPI network is thereafter re-weighted based on the learned protein representations. Finally, we perform protein identification on the re-weighted dynamic PPI network. Extensive experimental results demonstrate that DHPRL can effectively model complicated biological information and achieve state-of-the-art performance in most cases.
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