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异构网络模型鉴定与人类蛋白质之间潜在关联。

Heterogeneous Network Model to Identify Potential Associations Between and Human Proteins.

机构信息

Department of Mathematics, Faculty of Applied Science, King Mongkut's University of Technology North Bangkok, Bangkok 10800, Thailand.

Advanced Virtual and Intelligent Computing (AVIC) Center, Department of Mathematics and Computer Science, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Int J Mol Sci. 2020 Feb 15;21(4):1310. doi: 10.3390/ijms21041310.

Abstract

Integration of multiple sources and data levels provides a great insight into the complex associations between human and malaria systems. In this study, a meta-analysis framework was developed based on a heterogeneous network model for integrating human-malaria protein similarities, a human protein interaction network, and a protein interaction network. An iterative network propagation was performed on the heterogeneous network until we obtained stabilized weights. The association scores were calculated for qualifying a novel potential human-malaria protein association. This method provided a better performance compared to random experiments. After that, the stabilized network was clustered into association modules. The potential association candidates were then thoroughly analyzed by statistical enrichment analysis with protein complexes and known drug targets. The most promising target proteins were the succinate dehydrogenase protein complex in the human citrate (TCA) cycle pathway and the nicotinic acetylcholine receptor in the human central nervous system. Promising associations and potential drug targets were also provided for further studies and designs in therapeutic approaches for malaria at a systematic level. In conclusion, this method is efficient to identify new human-malaria protein associations and can be generalized to infer other types of association studies to further advance biomedical science.

摘要

整合多个来源和数据层次提供了对人类和疟疾系统之间复杂关联的深刻洞察。在这项研究中,我们基于一种异构网络模型开发了一种元分析框架,该模型整合了人类-疟疾蛋白相似性、人类蛋白质相互作用网络和蛋白质相互作用网络。在异构网络上进行迭代网络传播,直到获得稳定的权重。关联分数用于确定新的潜在人类-疟疾蛋白关联。与随机实验相比,该方法提供了更好的性能。然后,将稳定的网络聚类为关联模块。然后通过蛋白质复合物和已知药物靶点的统计富集分析对潜在的关联候选物进行全面分析。最有前途的靶蛋白是人类柠檬酸(TCA)循环途径中的琥珀酸脱氢蛋白复合物和人类中枢神经系统中的烟碱型乙酰胆碱受体。还为疟疾在系统水平上的治疗方法提供了有前途的关联和潜在的药物靶点,以进行进一步的研究和设计。总之,该方法可有效识别新的人类-疟疾蛋白关联,并可推广用于推断其他类型的关联研究,以进一步推进生物医学科学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/7072978/05c5cb63b918/ijms-21-01310-g001.jpg

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