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免疫信息学研究搜索 SARS-CoV-2 刺突糖蛋白表位作为潜在疫苗。

Immunoinformatics study to search epitopes of spike glycoprotein from SARS-CoV-2 as potential vaccine.

机构信息

Laboratorio de Diseño y Desarrollo de Nuevos Fármacos e Innovación Biotécnológica (Laboratory for the Design and Development of New Drugs and Biotechnological Innovation), Escuela Superior de Medicina, Instituto Politécnico Nacional, México City, México.

Laboratorio de medicina de Conservación, Escuela Superior de Medicina, Instituto Politécnico Nacional, México City, México.

出版信息

J Biomol Struct Dyn. 2021 Aug;39(13):4878-4892. doi: 10.1080/07391102.2020.1780944. Epub 2020 Jun 25.

DOI:10.1080/07391102.2020.1780944
PMID:32583729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7332869/
Abstract

The Coronavirus disease named COVID-19 is caused by the virus reported in 2019 first identified in China. The cases of this disease have increased and as of June 1, 2020 there are more than 216 countries affected. Pharmacological treatments have been proposed based on the resemblance of the HIV virus. With regard to prevention there is no vaccine, thus, we proposed to explore the spike protein due to its presence on the viral surface, and it also contains the putative viral entry receptor as well as the fusion peptide (important in the genome release). In this work we have employed techniques such as immunoinformatics tools which permit the identification of potential immunogenic regions on the viral surface (spike glycoprotein). From these analyses, we identified four epitopes E332-370, E627-651, E440-464 and E694-715 that accomplish essential features such as promiscuity, conservation grade, exposure and universality, and they also form stable complexes with MHCII molecule. We suggest that these epitopes could generate a specific immune response, and thus, they could be used for future applications such as the design of new epitope vaccines against the SARS-CoV-2.Communicated by Ramaswamy H. Sarma.

摘要

新型冠状病毒病(COVID-19)是由 2019 年在中国首次发现的病毒引起的。截至 2020 年 6 月 1 日,已有超过 216 个国家受到该疾病的影响。根据 HIV 病毒的相似性提出了药物治疗方法。关于预防,目前还没有疫苗,因此,我们提出探索病毒表面存在的刺突蛋白,因为它包含假定的病毒进入受体以及融合肽(在基因组释放中很重要)。在这项工作中,我们使用了免疫信息学工具等技术,可以识别病毒表面上的潜在免疫原性区域(刺突糖蛋白)。通过这些分析,我们确定了四个表位 E332-370、E627-651、E440-464 和 E694-715,它们具有变异性、保守性、暴露性和通用性等重要特征,并且与 MHCII 分子形成稳定的复合物。我们认为这些表位可以引发特异性免疫反应,因此可以用于未来的应用,例如设计针对 SARS-CoV-2 的新型表位疫苗。

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本文引用的文献

1
Genotyping coronavirus SARS-CoV-2: methods and implications.冠状病毒 SARS-CoV-2 的基因分型:方法与意义。
Genomics. 2020 Sep;112(5):3588-3596. doi: 10.1016/j.ygeno.2020.04.016. Epub 2020 Apr 27.
2
Comparative genetic analysis of the novel coronavirus (2019-nCoV/SARS-CoV-2) receptor ACE2 in different populations.新型冠状病毒(2019-nCoV/SARS-CoV-2)受体ACE2在不同人群中的比较遗传分析。
Cell Discov. 2020 Feb 24;6:11. doi: 10.1038/s41421-020-0147-1. eCollection 2020.
3
Analysis of angiotensin-converting enzyme 2 (ACE2) from different species sheds some light on cross-species receptor usage of a novel coronavirus 2019-nCoV.对不同物种的血管紧张素转换酶2(ACE2)进行分析,有助于了解新型冠状病毒2019-nCoV的跨物种受体使用情况。
J Infect. 2020 Apr;80(4):469-496. doi: 10.1016/j.jinf.2020.02.013. Epub 2020 Feb 21.
4
Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation.2019 年新型冠状病毒刺突蛋白在预融合构象的冷冻电镜结构
Science. 2020 Mar 13;367(6483):1260-1263. doi: 10.1126/science.abb2507. Epub 2020 Feb 19.
5
Emergence of SARS-like coronavirus poses new challenge in China.类似非典的冠状病毒的出现给中国带来了新挑战。
J Infect. 2020 Mar;80(3):350-371. doi: 10.1016/j.jinf.2020.01.017. Epub 2020 Jan 30.
6
Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding.新冠病毒的基因组特征和流行病学:对病毒起源和受体结合的影响。
Lancet. 2020 Feb 22;395(10224):565-574. doi: 10.1016/S0140-6736(20)30251-8. Epub 2020 Jan 30.
7
Receptor Recognition by the Novel Coronavirus from Wuhan: an Analysis Based on Decade-Long Structural Studies of SARS Coronavirus.新型冠状病毒受体识别:基于 SARS 冠状病毒长达十年结构研究的分析。
J Virol. 2020 Mar 17;94(7). doi: 10.1128/JVI.00127-20.
8
The Extent of Transmission of Novel Coronavirus in Wuhan, China, 2020.2020年中国武汉新型冠状病毒的传播范围
J Clin Med. 2020 Jan 24;9(2):330. doi: 10.3390/jcm9020330.
9
Cross-species transmission of the newly identified coronavirus 2019-nCoV.新型冠状病毒 2019-nCoV 的跨物种传播。
J Med Virol. 2020 Apr;92(4):433-440. doi: 10.1002/jmv.25682.
10
Origin and evolution of pathogenic coronaviruses.致病冠状病毒的起源与演化。
Nat Rev Microbiol. 2019 Mar;17(3):181-192. doi: 10.1038/s41579-018-0118-9.