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基于 SARS-CoV-2 包膜蛋白的免疫信息学分析评估对 COVID-19 的交叉保护作用

Immunoinformatic analysis of the SARS-CoV-2 envelope protein as a strategy to assess cross-protection against COVID-19.

机构信息

Department of Health Science, University "Magna Græcia" of Catanzaro, Viale Europa, 88100, Catanzaro, Italy.

Department of Biomedical, Surgical and Dental Sciences- One Health Unit, University of Milano, Via Celoria n10, 20133, Milano, Italy; Department of Veterinary Medicine, University of Milano, Via dell'Università 6, 26900, Lodi, Italy.

出版信息

Microbes Infect. 2020 May-Jun;22(4-5):182-187. doi: 10.1016/j.micinf.2020.05.013. Epub 2020 May 21.

Abstract

Envelope protein of coronaviruses is a structural protein existing in both monomeric and homo-pentameric form. It has been related to a multitude of roles including virus infection, replication, dissemination and immune response stimulation. In the present study, we employed an immunoinformatic approach to investigate the major immunogenic domains of the SARS-CoV-2 envelope protein and map them among the homologue proteins of coronaviruses with tropism for animal species that are closely inter-related with the human beings population all over the world. Also, when not available, we predicted the envelope protein structural folding and mapped SARS-CoV-2 epitopes. Envelope sequences alignment provides evidence of high sequence homology for some of the investigated virus specimens; while the structural mapping of epitopes resulted in the interesting maintenance of the structural folding and epitope sequence localization also in the envelope proteins scoring a lower alignment score. In line with the One-Health approach, our evidences provide a molecular structural rationale for a potential role of taxonomically related coronaviruses in conferring protection from SARS-CoV-2 infection and identifying potential candidates for the development of diagnostic tools and prophylactic-oriented strategies.

摘要

冠状病毒的包膜蛋白是一种结构蛋白,以单体和同源五聚体的形式存在。它与多种功能有关,包括病毒感染、复制、传播和免疫反应刺激。在本研究中,我们采用免疫信息学方法来研究 SARS-CoV-2 包膜蛋白的主要免疫原性结构域,并在对与世界各地人类密切相关的动物种具有嗜性的冠状病毒同源蛋白中对其进行定位。另外,当包膜蛋白结构折叠和 SARS-CoV-2 表位不可用时,我们对其进行预测。包膜序列比对为一些研究病毒样本提供了高序列同源性的证据;而表位的结构定位则有趣地保持了结构折叠和表位序列的定位,即使在包膜蛋白的比对得分较低的情况下也是如此。根据“同一健康”的方法,我们的证据为分类上相关的冠状病毒在提供针对 SARS-CoV-2 感染的保护和确定用于开发诊断工具和预防为导向的策略的潜在候选物方面的潜在作用提供了分子结构依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a83/7241347/d658dad25970/gr1_lrg.jpg

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