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探索流感和 COVID-19 的新抗病毒靶点:绘制病毒 RNA 聚合酶中有前景的热点。

Exploring new antiviral targets for influenza and COVID-19: Mapping promising hot spots in viral RNA polymerases.

机构信息

Host-Pathogen Interaction Unit, Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003, Lisbon, Portugal.

Host-Pathogen Interaction Unit, Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003, Lisbon, Portugal; Antiviral Resistance Lab, Research & Development Unit, Infectious Diseases Department, Instituto Nacional de Saúde Doutor Ricardo Jorge, IP, Av. Padre Cruz, 1649-016, Lisbon, Portugal.

出版信息

Virology. 2023 Jan;578:45-60. doi: 10.1016/j.virol.2022.11.001. Epub 2022 Nov 18.

Abstract

Influenza and COVID-19 are infectious respiratory diseases that represent a major concern to public health with social and economic impact worldwide, for which the available therapeutic options are not satisfactory. The RdRp has a central role in viral replication and thus represents a major target for the development of antiviral approaches. In this study, we focused on Influenza A virus PB1 polymerase protein and the betacoronaviruses nsp12 polymerase protein, considering their functional and structural similarities. We have performed conservation and druggability analysis to map conserved druggable regions, that may have functional or structural importance in these proteins. We disclosed the most promising and new targeting regions for the discovery of new potential polymerase inhibitors. Conserved druggable regions of putative interaction with favipiravir and molnupiravir were also mapped. We have also compared and integrated the current findings with previous research.

摘要

流感和 COVID-19 是具有传染性的呼吸道疾病,对全球公共卫生和经济造成重大影响,而目前的治疗选择并不令人满意。RdRp 在病毒复制中起核心作用,因此是开发抗病毒方法的主要靶点。在这项研究中,我们专注于流感 A 病毒 PB1 聚合酶蛋白和β冠状病毒 nsp12 聚合酶蛋白,考虑到它们的功能和结构相似性。我们进行了保守性和可成药性分析,以绘制可能在这些蛋白中具有功能或结构重要性的保守可成药区域。我们揭示了最有前途和新的针对聚合酶抑制剂发现的新靶标区域。还绘制了与法匹拉韦和莫那比拉韦具有假定相互作用的保守可成药区域。我们还比较和整合了目前的研究结果与以前的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d39/9674405/63283391680a/ga1_lrg.jpg

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