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SARS-CoV-2 的包膜(E)蛋白作为药物作用靶点。

The Envelope (E) Protein of SARS-CoV-2 as a Pharmacological Target.

机构信息

Laboratory of Transcriptomics and Molecular Immunology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.

出版信息

Viruses. 2023 Apr 19;15(4):1000. doi: 10.3390/v15041000.

Abstract

The COVID-19 pandemic caused by the SARS-CoV-2 virus is still a global health concern. Several spike (S) protein-based vaccines have been developed that efficiently protect the human population against severe forms of COVID-19. However, some SARS-CoV-2 variants of concern (VOCs) have emerged that evade the protective effect of vaccine-induced antibodies. Therefore, efficient and specific antiviral treatments to control COVID-19 are indispensable. To date, two drugs have been approved for mild COVID-19 treatment; nevertheless, more drugs, preferably broad-spectrum and ready-to-use therapeutic agents for new pandemics, are needed. Here, I discuss the PDZ-dependent protein-protein interactions of the viral E protein with host proteins as attractive alternatives for the development of antivirals against coronavirus.

摘要

由 SARS-CoV-2 病毒引起的 COVID-19 大流行仍然是全球关注的健康问题。已经开发出了几种基于刺突(S)蛋白的疫苗,这些疫苗有效地保护了人类免受 COVID-19 的严重形式的侵害。然而,一些令人关注的 SARS-CoV-2 变体(VOC)已经出现,逃避了疫苗诱导的抗体的保护作用。因此,高效和特异的抗病毒治疗对于控制 COVID-19 是不可或缺的。迄今为止,已有两种药物被批准用于轻度 COVID-19 的治疗;然而,需要更多的药物,最好是广谱的、可用于新大流行的即用型治疗药物。在这里,我讨论了病毒 E 蛋白与宿主蛋白的 PDZ 依赖性蛋白-蛋白相互作用,作为开发针对冠状病毒的抗病毒药物的有吸引力的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79fe/10143767/566308915973/viruses-15-01000-g001.jpg

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