Suppr超能文献

对冠状病毒 SARS-CoV-2(COVID-19)感染机制和选择性的理论研究。

Theoretical Investigation of the Coronavirus SARS-CoV-2 (COVID-19) Infection Mechanism and Selectivity.

机构信息

Faculty of Chemistry, University of Gdansk, ul. Wita Stwosza 63, 80-308 Gdansk, Poland.

出版信息

Molecules. 2022 Mar 24;27(7):2080. doi: 10.3390/molecules27072080.

Abstract

The SARS-CoV-2 virus, commonly known as COVID-19, first occurred in December 2019 in Wuhan, Hubei Province, China. Since then, it has become a tremendous threat to human health. With a pandemic threat, it is in the significant interest of the scientific world to establish its method of infection. In this manuscript, we combine knowledge of the infection mechanism with theoretical methods to answer the question of the virus's selectivity. We proposed a two-stage infection mechanism. In the first step, the virus interacts with the ACE2 receptor, with the "proper strength". When the interaction is too strong, the virus will remain in an "improper position"; if the interaction is too weak, the virus will "run away" from the cell. We also indicated three residues (positions 30, 31, and 353) located on the ACE2 protein-binding interface, which seems to be crucial for successful infection. Our results indicate that these residues are necessary for the initiation of the infection process.

摘要

SARS-CoV-2 病毒,通常被称为 COVID-19,于 2019 年 12 月在中国湖北省武汉市首次出现。自那时以来,它已成为对人类健康的巨大威胁。由于存在大流行的威胁,确定其感染方法符合科学界的重大利益。在本文中,我们将感染机制的知识与理论方法相结合,回答了病毒选择性的问题。我们提出了一个两阶段感染机制。在第一步中,病毒与 ACE2 受体相互作用,具有“适当的强度”。当相互作用过强时,病毒将保持在“不当位置”;如果相互作用太弱,病毒将“逃离”细胞。我们还指出了位于 ACE2 蛋白结合界面上的三个残基(位置 30、31 和 353),它们似乎对成功感染至关重要。我们的结果表明,这些残基对于感染过程的开始是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09bd/9000624/a655aded3552/molecules-27-02080-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验