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RAN 抑制可减弱甲型流感病毒复制和核蛋白核输出。

Inhibition of RAN attenuates influenza a virus replication and nucleoprotein nuclear export.

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, People's Republic of China.

College of Animal Medicine, Huazhong Agricultural University, Wuhan, People's Republic of China.

出版信息

Emerg Microbes Infect. 2024 Dec;13(1):2387910. doi: 10.1080/22221751.2024.2387910. Epub 2024 Aug 12.

Abstract

Nuclear export of the viral ribonucleoprotein (vRNP) is a critical step in the influenza A virus (IAV) life cycle and may be an effective target for the development of anti-IAV drugs. The host factor ras-related nuclear protein (RAN) is known to participate in the life cycle of several viruses, but its role in influenza virus replication remains unknown. In the present study, we aimed to determine the function of RAN in influenza virus replication using different cell lines and subtype strains. We found that RAN is essential for the nuclear export of vRNP, as it enhances the binding affinity of XPO1 toward the viral nuclear export protein NS2. Depletion of RAN constrained the vRNP complex in the nucleus and attenuated the replication of various subtypes of influenza virus. Using in silico compound screening, we identified that bepotastine could dissociate the RAN-XPO1-vRNP trimeric complex and exhibit potent antiviral activity against influenza virus both and . This study demonstrates the important role of RAN in IAV replication and suggests its potential use as an antiviral target.

摘要

病毒核糖核蛋白(vRNP)的核输出是甲型流感病毒(IAV)生命周期中的一个关键步骤,可能是开发抗 IAV 药物的有效靶点。宿主因子 ras 相关核蛋白(RAN)已知参与几种病毒的生命周期,但它在流感病毒复制中的作用尚不清楚。在本研究中,我们旨在使用不同的细胞系和亚型毒株来确定 RAN 在流感病毒复制中的功能。我们发现 RAN 对于 vRNP 的核输出是必不可少的,因为它增强了 XPO1 与病毒核输出蛋白 NS2 的结合亲和力。RAN 的耗竭将 vRNP 复合物限制在核内,并减弱了各种亚型流感病毒的复制。通过计算机化合物筛选,我们发现 bepotastine 可以解离 RAN-XPO1-vRNP 三聚体复合物,并对 和 具有强大的抗流感病毒活性。这项研究表明 RAN 在 IAV 复制中的重要作用,并暗示其可能作为抗病毒靶点的用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d8/11321118/d2c6e259290d/TEMI_A_2387910_F0001_OC.jpg

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