爱泼斯坦-巴氏病毒:人类相互作用组揭示了病毒发病机制的新分子观点,有助于潜在治疗和抗病毒药物的发现。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-01-01 Epub Date: 2024-01-08 DOI:10.1089/omi.2023.0241
Deepak Krishnan, Sreeranjini Babu, Rajesh Raju, Mohanan Valiya Veettil, Thottethodi Subramanya Keshava Prasad, Chandran S Abhinand
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引用次数: 0

摘要

宿主-病毒蛋白质-蛋白质相互作用(PPIs)在对病毒致病至关重要的生物过程中发挥着关键作用,进而为抗病毒药物的发现和治疗创新提供信息。尽管人们努力开发爱泼斯坦-巴尔病毒(EBV)-宿主 PPI 网络,但仍然存在巨大的知识差距,已破译的相互作用人类蛋白质数量有限。此外,人们对 EBV-宿主 PPI 网络在不同的溶解和潜伏病毒阶段的动态变化仍然一无所知。在这项研究中,我们通过整合公共数据库 HPIDB(v3.0)中的数据以及文献中的高通量蛋白质组数据,报告了一个全面的 EBV-人类蛋白质相互作用图谱,其中包括 1752 个人类蛋白质和 61 个 EBV 蛋白质。针对 EBV 感染的阶段特异性,我们生成了代表潜伏期和成熟期的两个详细子集网络,分别包含 747 和 481 个人类蛋白质。对这些子集进行的功能和通路富集分析揭示了 EBV 蛋白对癌症的深远影响。高度关联蛋白质的鉴定以及内在紊乱和癌症相关蛋白质的特征描述,为潜在的治疗靶点提供了宝贵的见解。此外,对药物-蛋白质相互作用的探索揭示了枢纽蛋白与抗癌药物之间的显著关联,为控制 EBV 发病机制提供了新的视角。据我们所知,这项研究是首次利用高通量数据集对 EBV 感染的两个不同阶段进行的全面调查。这有助于我们理解 EBV 与宿主的相互作用,并为未来的药物发现和治疗干预奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epstein-Barr Virus: Human Interactome Reveals New Molecular Insights into Viral Pathogenesis for Potential Therapeutics and Antiviral Drug Discovery.

Host-virus Protein-Protein Interactions (PPIs) play pivotal roles in biological processes crucial for viral pathogenesis and by extension, inform antiviral drug discovery and therapeutics innovations. Despite efforts to develop the Epstein-Barr virus (EBV)-host PPI network, there remain significant knowledge gaps and a limited number of interacting human proteins deciphered. Furthermore, understanding the dynamics of the EBV-host PPI network in the distinct lytic and latent viral stages remains elusive. In this study, we report a comprehensive map of the EBV-human protein interactions, encompassing 1752 human and 61 EBV proteins by integrating data from the public repository HPIDB (v3.0) as well as curated high-throughput proteomic data from the literature. To address the stage-specific nature of EBV infection, we generated two detailed subset networks representing the latent and lytic stages, comprising 747 and 481 human proteins, respectively. Functional and pathway enrichment analysis of these subsets uncovered the profound impact of EBV proteins on cancer. The identification of highly connected proteins and the characterization of intrinsically disordered and cancer-related proteins provide valuable insights into potential therapeutic targets. Moreover, the exploration of drug-protein interactions revealed notable associations between hub proteins and anticancer drugs, offering novel perspectives for controlling EBV pathogenesis. This study represents, to the best of our knowledge, the first comprehensive investigation of the two distinct stages of EBV infection using high-throughput datasets. This makes a contribution to our understanding of EBV-host interactions and provides a foundation for future drug discovery and therapeutic interventions.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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