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使用公开可用的生物信息学工具研究冠状病毒:以病毒结构蛋白为例

Scrutinizing Coronaviruses Using Publicly Available Bioinformatic Tools: The Viral Structural Proteins as a Case Study.

作者信息

Beeckmans Sonia, Van Driessche Edilbert

机构信息

Research Unit Protein Chemistry, Vrije Universiteit Brussel, Brussels, Belgium.

出版信息

Front Mol Biosci. 2021 May 24;8:671923. doi: 10.3389/fmolb.2021.671923. eCollection 2021.

Abstract

Since early 2020, the world suffers from a new beta-coronavirus, called SARS-CoV-2, that has devastating effects globally due to its associated disease, Covid-19. Until today, Covid-19, which not only causes life-threatening lung infections but also impairs various other organs and tissues, has killed hundreds of thousands of people and caused irreparable damage to many others. Since the very onset of the pandemic, huge efforts were made worldwide to fully understand this virus and numerous studies were, and still are, published. Many of these deal with structural analyses of the viral spike glycoprotein and with vaccine development, antibodies and antiviral molecules or immunomodulators that are assumed to become essential tools in the struggle against the virus. This paper summarizes knowledge on the properties of the four structural proteins (spike protein S, membrane protein M, envelope protein E and nucleocapsid protein N) of the SARS-CoV-2 virus and its relatives, SARS-CoV and MERS-CoV, that emerged few years earlier. Moreover, attention is paid to ways to analyze such proteins using freely available bioinformatic tools and, more importantly, to bring these proteins alive by looking at them on a computer/laptop screen with the easy-to-use but highly performant and interactive molecular graphics program DeepView. It is hoped that this paper will stimulate non-bioinformaticians and non-specialists in structural biology to scrutinize these and other macromolecules and as such will contribute to establishing procedures to fight these and maybe other forthcoming viruses.

摘要

自2020年初以来,全球遭受一种新型β冠状病毒——严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的侵袭,其所引发的疾病——2019冠状病毒病(Covid-19)在全球造成了毁灭性影响。截至目前,Covid-19不仅会引发危及生命的肺部感染,还会损害其他各种器官和组织,已导致数十万人死亡,并给许多其他人造成了无法弥补的损害。自疫情爆发之初,全球便付出了巨大努力来全面了解这种病毒,并且已经发表了大量研究,而且仍在不断发表。其中许多研究涉及病毒刺突糖蛋白的结构分析以及疫苗开发、抗体、抗病毒分子或免疫调节剂,这些被认为将成为抗击该病毒的关键工具。本文总结了有关SARS-CoV-2病毒及其几年前出现的亲属——严重急性呼吸综合征冠状病毒(SARS-CoV)和中东呼吸综合征冠状病毒(MERS-CoV)的四种结构蛋白(刺突蛋白S、膜蛋白M、包膜蛋白E和核衣壳蛋白N)特性的知识。此外,还介绍了使用免费生物信息学工具分析此类蛋白质的方法,更重要的是,通过使用易于使用但性能强大且具有交互性的分子图形程序DeepView在计算机/笔记本电脑屏幕上查看这些蛋白质,使其“活灵活现”。希望本文能激发非生物信息学家和结构生物学非专家对这些及其他大分子进行仔细研究,从而有助于建立对抗这些以及可能出现的其他病毒的程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ca/8181738/b71c1b2e06df/fmolb-08-671923-g001.jpg

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