Proteomics research of SARS-CoV-2 and COVID-19 disease.

Medical review (Berlin, Germany) Pub Date : 2022-09-14 eCollection Date: 2022-08-01 DOI:10.1515/mr-2022-0016
Nan Zhang, Siyuan Wang, Catherine C L Wong
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引用次数: 0

Abstract

Currently, coronavirus disease 2019 (COVID-19) is still spreading in a global scale, exerting a massive health and socioeconomic crisis. Deep insights into the molecular functions of the viral proteins and the pathogenesis of this infectious disease are urgently needed. In this review, we comprehensively describe the proteome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and summarize their protein interaction map with host cells. In the protein interaction network between the virus and the host, a total of 787 host prey proteins that appeared in at least two studies or were verified by co-immunoprecipitation experiments. Together with 29 viral proteins, a network of 1762 proximal interactions were observed. We also review the proteomics results of COVID-19 patients and proved that SARS-CoV-2 hijacked the host's translation system, post-translation modification system, and energy supply system via viral proteins, resulting in various immune disorders, multiple cardiomyopathies, and cholesterol metabolism diseases.

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SARS-CoV-2和新冠肺炎疾病的蛋白质组学研究。
目前,2019冠状病毒病(新冠肺炎)仍在全球范围内传播,造成了巨大的健康和社会经济危机。迫切需要深入了解病毒蛋白的分子功能和这种传染病的发病机制。在这篇综述中,我们全面描述了严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)的蛋白质组,并总结了它们与宿主细胞的蛋白质相互作用图。在病毒和宿主之间的蛋白质相互作用网络中,共有787种宿主猎物蛋白质出现在至少两项研究中,或通过免疫共沉淀实验验证。与29种病毒蛋白一起,观察到1762种近端相互作用的网络。我们还回顾了新冠肺炎患者的蛋白质组学结果,证明了SARS-CoV-2通过病毒蛋白劫持了宿主的翻译系统、翻译后修饰系统和能量供应系统,导致各种免疫疾病、多种心肌疾病和胆固醇代谢疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.30
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