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N-糖蛋白质组学分析揭示了可能参与千金藤素干预的新型冠状病毒治疗靶点。

N-glycoproteomic profiling revealing novel coronavirus therapeutic targets potentially involved in Cepharanthine's intervention.

作者信息

An Wenlin, Tian Fengjuan, Li Jing, Chen Junge, Tong Yigang

机构信息

College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 10029, China.

National Vaccine & Serum Institute (NVSI), China National Biotech Group (CNBG), 38 JingHai Second Road, Beijing, 101111, China.

出版信息

Med Nov Technol Devices. 2022 Dec;16:100156. doi: 10.1016/j.medntd.2022.100156. Epub 2022 Jul 21.

Abstract

The Coronavirus disease 2019 (COVID-19) has posed a serious threat to global health and the world economy. Antiviral therapies targeting coronavirus are urgently required. The Cepharanthine (CEP) is a traditional Chinese herbal extract. Our previous research revealed that CEP has a very potent anti-coronavirus effect, but its mechanism of action was not fully understood. To investigate the effect of novel coronavirus on protein glycosylation in infected cells and to further investigate the mechanism of action of CEP against coronavirus, a cellular model using coronavirus GX_P2V infection of Vero E6 cells was established. The effect of coronavirus GX_P2V on host cell protein glycosylation was investigated by N-glycoproteomic analysis, and the antagonistic effect of CEP on the abnormal protein glycosylation caused by coronavirus was analyzed. The results showed that GX_P2V could cause abnormal changes in protein glycosylation levels in host cells, while CEP could partially antagonize the abnormal protein glycosylation caused by GX_P2V. In addition, we also found that CEP could regulate the glycosylation level of coronavirus S protein. In conclusion, this article provides important ideas about the infection mechanism of novel coronaviruses, providing evidence for CEP as a promising therapeutic option for coronavirus infection.

摘要

2019年冠状病毒病(COVID-19)对全球健康和世界经济构成了严重威胁。迫切需要针对冠状病毒的抗病毒疗法。千金藤素(CEP)是一种传统的中草药提取物。我们之前的研究表明,CEP具有非常强大的抗冠状病毒作用,但其作用机制尚不完全清楚。为了研究新型冠状病毒对感染细胞中蛋白质糖基化的影响,并进一步探究CEP抗冠状病毒的作用机制,建立了冠状病毒GX_P2V感染Vero E6细胞的细胞模型。通过N-糖蛋白质组学分析研究冠状病毒GX_P2V对宿主细胞蛋白质糖基化的影响,并分析CEP对冠状病毒引起的异常蛋白质糖基化的拮抗作用。结果表明,GX_P2V可导致宿主细胞蛋白质糖基化水平发生异常变化,而CEP可部分拮抗GX_P2V引起的异常蛋白质糖基化。此外,我们还发现CEP可调节冠状病毒S蛋白的糖基化水平。总之,本文为新型冠状病毒的感染机制提供了重要思路,为CEP作为冠状病毒感染的一种有前景的治疗选择提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35ee/9301903/82f36ea9e20b/gr1_lrg.jpg

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