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COVID-19 疫情爆发:历史、机制、传播、结构研究和治疗。

COVID-19 outbreak: history, mechanism, transmission, structural studies and therapeutics.

机构信息

Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology Madras, Chennai, 600036, India.

School of Computing, Tokyo Tech World Research Hub Initiative (WRHI), Institute of Innovative Research, Tokyo Institute of Technology, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.

出版信息

Infection. 2021 Apr;49(2):199-213. doi: 10.1007/s15010-020-01516-2. Epub 2020 Sep 4.

Abstract

PURPOSE

The coronavirus outbreak emerged as a severe pandemic, claiming more than 0.8 million lives across the world and raised a major global health concern. We survey the history and mechanism of coronaviruses, and the structural characteristics of the spike protein and its key residues responsible for human transmissions.

METHODS

We have carried out a systematic review to summarize the origin, transmission and etiology of COVID-19. The structural analysis of the spike protein and its disordered residues explains the mechanism of the viral transmission. A meta-data analysis of the therapeutic compounds targeting the SARS-CoV-2 is also included.

RESULTS

Coronaviruses can cross the species barrier and infect humans with unexpected consequences for public health. The transmission rate of SARS-CoV-2 infection is higher compared to that of the closely related SARS-CoV infections. In SARS-CoV-2 infection, intrinsically disordered regions are observed at the interface of the spike protein and ACE2 receptor, providing a shape complementarity to the complex. The key residues of the spike protein have stronger binding affinity with ACE2. These can be probable reasons for the higher transmission rate of SARS-CoV-2. In addition, we have also discussed the therapeutic compounds and the vaccines to target SARS-CoV-2, which can help researchers to develop effective drugs/vaccines for COVID-19. The overall history and mechanism of entry of SARS-CoV-2 along with structural study of spike-ACE2 complex provide insights to understand disease pathogenesis and development of vaccines and drugs.

摘要

目的

冠状病毒的爆发成为了一场严重的大流行病,在全球范围内造成了超过 80 万人死亡,引起了全球重大的健康关注。我们调查了冠状病毒的历史和机制,以及刺突蛋白的结构特征及其负责人际传播的关键残基。

方法

我们进行了系统综述,以总结 COVID-19 的起源、传播和病因。刺突蛋白及其无规卷曲残基的结构分析解释了病毒传播的机制。还包括针对 SARS-CoV-2 的治疗化合物的元数据分析。

结果

冠状病毒可以跨越物种屏障并感染人类,对公共卫生造成意想不到的后果。与密切相关的 SARS-CoV 感染相比,SARS-CoV-2 感染的传播率更高。在 SARS-CoV-2 感染中,观察到刺突蛋白和 ACE2 受体界面处存在固有无序区域,为复合物提供了形状互补性。刺突蛋白的关键残基与 ACE2 具有更强的结合亲和力。这些可能是 SARS-CoV-2 传播率更高的原因。此外,我们还讨论了针对 SARS-CoV-2 的治疗化合物和疫苗,这可以帮助研究人员为 COVID-19 开发有效的药物/疫苗。SARS-CoV-2 的进入的总体历史和机制以及刺突-ACE2 复合物的结构研究为了解疾病发病机制和疫苗及药物的开发提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/7472674/d59173140b47/15010_2020_1516_Fig1_HTML.jpg

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