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氧化石墨烯纳米片与 SARS-CoV-2 表面蛋白和细胞受体相互作用和干扰,以抑制感染性。

Graphene Oxide Nanosheets Interact and Interfere with SARS-CoV-2 Surface Proteins and Cell Receptors to Inhibit Infectivity.

机构信息

Stem Cell Institute, Ankara University, Balgat, Ankara, 06520, Turkey.

Ministry of Health General Directorate of Public Health, Microbiology References Laboratory, Sihhiye, Ankara, 06430, Turkey.

出版信息

Small. 2021 Jun;17(25):e2101483. doi: 10.1002/smll.202101483. Epub 2021 May 14.

Abstract

Nanotechnology can offer a number of options against coronavirus disease 2019 (COVID-19) acting both extracellularly and intracellularly to the host cells. Here, the aim is to explore graphene oxide (GO), the most studied 2D nanomaterial in biomedical applications, as a nanoscale platform for interaction with SARS-CoV-2. Molecular docking analyses of GO sheets on interaction with three different structures: SARS-CoV-2 viral spike (open state - 6VYB or closed state - 6VXX), ACE2 (1R42), and the ACE2-bound spike complex (6M0J) are performed. GO shows high affinity for the surface of all three structures (6M0J, 6VYB and 6VXX). When binding affinities and involved bonding types are compared, GO interacts more strongly with the spike or ACE2, compared to 6M0J. Infection experiments using infectious viral particles from four different clades as classified by Global Initiative on Sharing all Influenza Data (GISAID), are performed for validation purposes. Thin, biological-grade GO nanoscale (few hundred nanometers in lateral dimension) sheets are able to significantly reduce copies for three different viral clades. This data has demonstrated that GO sheets have the capacity to interact with SARS-CoV-2 surface components and disrupt infectivity even in the presence of any mutations on the viral spike. GO nanosheets are proposed to be further explored as a nanoscale platform for development of antiviral strategies against COVID-19.

摘要

纳米技术可以提供多种针对 2019 年冠状病毒病(COVID-19)的选择,既能在细胞外作用于宿主细胞,也能在细胞内作用于宿主细胞。在此,我们的目的是探索氧化石墨烯(GO),作为在生物医学应用中研究最多的二维纳米材料,作为与 SARS-CoV-2 相互作用的纳米级平台。对 GO 薄片与三种不同结构(SARS-CoV-2 病毒刺突(开放状态 - 6VYB 或关闭状态 - 6VXX)、ACE2(1R42)和 ACE2 结合的刺突复合物(6M0J))相互作用的分子对接分析。GO 表现出对所有三种结构(6M0J、6VYB 和 6VXX)表面的高亲和力。当比较结合亲和力和涉及的键合类型时,与 6M0J 相比,GO 与刺突或 ACE2 的相互作用更强。为了验证目的,进行了使用来自全球流感共享倡议组织(GISAID)分类的四个不同谱系的传染性病毒颗粒的感染实验。薄的、生物级 GO 纳米片(横向尺寸几百纳米)能够显著减少三种不同病毒谱系的拷贝数。这些数据表明,GO 薄片能够与 SARS-CoV-2 表面成分相互作用,并破坏感染性,即使在病毒刺突上存在任何突变的情况下也是如此。GO 纳米片被提议进一步探索作为开发针对 COVID-19 的抗病毒策略的纳米级平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bc/8236978/e5b96ae0ba53/SMLL-17-2101483-g006.jpg

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