De Novo设计的肽阻止SARS-CoV-2与宿主细胞上ACE2受体的相互作用

I. Cosic, U. Kuhar, U. Krapež, B. Slavec, D. Cosic, I. Loncarevic
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引用次数: 2

摘要

:肆虐全球的新冠肺炎大流行是由单链RNA病毒SARS-C0V-2引起的。这种病毒通过与宿主细胞表面的血管紧张素转换酶2 (ACE2)受体相互作用来攻击细胞。利用共振识别模型(RRM),我们设计了六个新的肽来防止这种相互作用。通过标准抑制剂筛选测定试剂盒对肽进行了预选,并提出了一种设计的肽(CovA)作为细胞系测试的良好候选肽。利用Vero E6细胞系,肽CovA显示出显著阻止SARS-CoV-2病毒与ACE2受体相互作用的能力。因此,设计的肽CovA可为新型COVID-19药物的开发提供基础。此外,这些结果支持RRM模型设计具有所需生物学功能的肽的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De Novo Designed Peptide to Prevent SARS-CoV-2 Interaction with ACE2 Receptor on Host Cells
: COVID-19 pandemic, which has made havoc in the World, is caused by single stranded RNA virus SARS-C0V-2. This virus attacks cells by interacting with Angiotensin-Converting Enzyme 2 (ACE2) receptor on the surface of host cells. Using the Resonant Recognition Model (RRM), we have designed six de novo peptides which are proposed to prevent this interaction. Peptide preselection has been by standard Inhibitor Screening Assay Kits and one of the designed peptides (CovA) has been proposed to be a good candidate for testing on cell lines. Using Vero E6 cell line, peptide CovA has shown ability to significantly prevent interaction between SARS-CoV-2 virus and ACE2 receptor. Thus, the designed peptide CovA could provide the basis for development of new COVID-19 drugs. In addition, these results are supporting the RRM model ability to design peptides with desired biological function.
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