Heat shock protein 90 facilitates SARS-CoV-2 structural protein-mediated virion assembly and promotes virus- induced pyroptosis

文献类型： 外文期刊

第一作者： Zhao, Zhuangzhuang

作者： Zhao, Zhuangzhuang;Jiao, Yajuan;Shi, Fang-Shu;Huang, Yao-Wei;Zhao, Zhuangzhuang;Liang, Qi-Zhang;Jiao, Yajuan;Shi, Fang-Shu;Huang, Yao-Wei;Xu, Ling-Dong;Zhang, Fei;Xu, Pinglong;Xu, Ling-Dong;Zhang, Fei;Xu, Pinglong;He, Biao

作者机构：

期刊名称：JOURNAL OF BIOLOGICAL CHEMISTRY （ 影响因子：4.8； 五年影响因子：4.8 ）

ISSN：

年卷期： 2023 年 299 卷 5 期

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收录情况： SCI

摘要： Inhibition of heat shock protein 90 (Hsp90), a prominent molecular chaperone, effectively limits severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection but little is known about any interaction between Hsp90 and SARS-CoV-2 proteins. Here, we systematically analyzed the effects of the chaperone isoforms Hsp90 alpha and Hsp9011 on individual SARSCoV-2 viral proteins. Five SARS-CoV-2 proteins, namely nucleocapsid (N), membrane (M), and accessory proteins Orf3, Orf7a, and Orf7b were found to be novel clients of Hsp9011 in particular. Pharmacological inhibition of Hsp90 with 17-DMAG results in N protein proteasome-dependent degradation. Hsp90 depletion-induced N protein degradation is independent of CHIP, a ubiquitin E3 ligase previously identified for Hsp90 client proteins, but alleviated by FBXO10, an E3 ligase identified by subsequent siRNA screening. We also provide evidence that Hsp90 depletion may suppress SARS-CoV-2 assembly partially through induced M or N degradation. Additionally, we found that GSDMD-mediated pyroptotic cell death triggered by SARSCoV-2 was mitigated by inhibition of Hsp90. These findings collectively highlight a beneficial role for targeting of Hsp90 during SARS-CoV-2 infection, directly inhibiting virion production and reducing inflammatory injury by preventing the pyroptosis that contributes to severe SARS-CoV-2 disease.

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