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抑制 HECT E3 连接酶可作为 COVID-19 的潜在治疗方法。

Inhibition of HECT E3 ligases as potential therapy for COVID-19.

机构信息

Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133, Rome, Italy.

IRCCS Neuromed, Pozzilli, (IS), Italy.

出版信息

Cell Death Dis. 2021 Mar 24;12(4):310. doi: 10.1038/s41419-021-03513-1.

Abstract

SARS-CoV-2 is responsible for the ongoing world-wide pandemic which has already taken more than two million lives. Effective treatments are urgently needed. The enzymatic activity of the HECT-E3 ligase family members has been implicated in the cell egression phase of deadly RNA viruses such as Ebola through direct interaction of its VP40 Protein. Here we report that HECT-E3 ligase family members such as NEDD4 and WWP1 interact with and ubiquitylate the SARS-CoV-2 Spike protein. Furthermore, we find that HECT family members are overexpressed in primary samples derived from COVID-19 infected patients and COVID-19 mouse models. Importantly, rare germline activating variants in the NEDD4 and WWP1 genes are associated with severe COVID-19 cases. Critically, I3C, a natural NEDD4 and WWP1 inhibitor from Brassicaceae, displays potent antiviral effects and inhibits viral egression. In conclusion, we identify the HECT family members of E3 ligases as likely novel biomarkers for COVID-19, as well as new potential targets of therapeutic strategy easily testable in clinical trials in view of the established well-tolerated nature of the Brassicaceae natural compounds.

摘要

SARS-CoV-2 是导致目前全球大流行的元凶,它已导致超过 200 万人死亡。目前急需有效的治疗方法。HECT-E3 连接酶家族成员的酶活性已被认为与埃博拉等致命 RNA 病毒的细胞外吐阶段有关,这是通过其 VP40 蛋白的直接相互作用实现的。在这里,我们报告称,HECT-E3 连接酶家族成员,如 NEDD4 和 WWP1,与 SARS-CoV-2 的 Spike 蛋白相互作用并使其泛素化。此外,我们发现 HECT 家族成员在源自 COVID-19 感染患者和 COVID-19 小鼠模型的原发性样本中过度表达。重要的是,NEDD4 和 WWP1 基因中的罕见种系激活变异与严重的 COVID-19 病例有关。至关重要的是,来自十字花科植物的天然 NEDD4 和 WWP1 抑制剂 I3C 显示出强大的抗病毒作用,并抑制病毒外吐。总之,我们确定 E3 连接酶的 HECT 家族成员可能是 COVID-19 的新型生物标志物,以及鉴于十字花科天然化合物的良好耐受性已得到确立,很容易在临床试验中进行测试的新的潜在治疗策略靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b8d/7991658/a535097ae49e/41419_2021_3513_Fig1_HTML.jpg

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