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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.

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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