基于蛋白质相互作用网络局部拓扑结构的宿主-病原体蛋白质相互作用预测

Jira Jindalertudomdee, M. Hayashida, Jiangning Song, T. Akutsu
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引用次数: 2

摘要

了解病原体蛋白如何与宿主蛋白相互作用是了解病原体感染机制的关键概念,这可能导致发现治疗传染病的改进疗法。几项研究表明,来自不同病原体的蛋白质倾向于与参与同一生物途径的人类蛋白质相互作用。这意味着病原体倾向于以具有相似功能的宿主蛋白质为目标。此外,在蛋白质-蛋白质相互作用网络(PIN)中,蛋白质的功能与其局部拓扑结构之间的守恒性已经被表征。这导致了一种假设,即病原体在PIN中以具有类似局部拓扑结构的宿主蛋白质为目标。在这项工作中,通过在预测模型中添加人类PIN中蛋白质的石墨烯度载体作为特征,并使用该模型预测人类与四种病原体之间的蛋白质-蛋白质相互作用,来检验这一假设。结果表明,该石墨烯度载体对所有病原菌的检测性能均有显著提高。这提示在开发宿主-病原体蛋白质相互作用预测方法时应考虑种内蛋白质-蛋白质相互作用。这些结果也支持了蛋白质的功能和PIN的局部拓扑之间存在关系的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host-Pathogen Protein Interaction Prediction Based on Local Topology Structures of a Protein Interaction Network
Understanding how pathogen's proteins interact with its host's proteins is the key concept for understanding pathogen's infection mechanism, which can lead to the discovery of improved therapeutics for treating infectious diseases. Several studies suggest that proteins from various pathogens tend to interact with human proteins involved in the same biological pathway. This implies that pathogens are inclined to target host's proteins with similar function. In addition, conservation between a protein's function and its local topological structure in a protein-protein interaction network (PIN) has been previously characterized. This leads to the hypothesis that pathogens target the host's proteins with a similar local topological structure in a PIN. In this work, this hypothesis is examined by adding a graphlet degree vector of a protein in the human PIN as a feature in the prediction model and using that model to predict the protein-protein interaction between human and four pathogens. The results show that this graphlet degree vector increases the performance significantly for all pathogens. This suggests that the intraspecies protein-protein interactions should be taken into consideration when developing prediction methods for host-pathogen protein interaction. The results also support the hypothesis that there exists a relationship between a protein's function and the local topology of the PIN.
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