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基于刺突纳米颗粒的具有双重作用模式的流感中和抑制剂的拓扑匹配设计。

Topology-Matching Design of an Influenza-Neutralizing Spiky Nanoparticle-Based Inhibitor with a Dual Mode of Action.

机构信息

Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustr. 3, 14195, Berlin, Germany.

Unit 17, Robert Koch Institut, Seestr. 10, 13353, Berlin, Germany.

出版信息

Angew Chem Int Ed Engl. 2020 Sep 1;59(36):15532-15536. doi: 10.1002/anie.202004832. Epub 2020 Jul 8.

Abstract

In this study, we demonstrate the concept of "topology-matching design" for virus inhibitors. With the current knowledge of influenza A virus (IAV), we designed a nanoparticle-based inhibitor (nano-inhibitor) that has a matched nanotopology to IAV virions and shows heteromultivalent inhibitory effects on hemagglutinin and neuraminidase. The synthesized nano-inhibitor can neutralize the viral particle extracellularly and block its attachment and entry to the host cells. The virus replication was significantly reduced by 6 orders of magnitude in the presence of the reverse designed nano-inhibitors. Even when used 24 hours after the infection, more than 99.999 % inhibition is still achieved, which indicates such a nano-inhibitor might be a potent antiviral for the treatment of influenza infection.

摘要

在这项研究中,我们展示了一种用于病毒抑制剂的“拓扑匹配设计”概念。基于我们对甲型流感病毒(IAV)的现有认识,我们设计了一种基于纳米粒子的抑制剂(纳米抑制剂),它的纳米拓扑结构与 IAV 病毒粒子相匹配,并对血凝素和神经氨酸酶表现出杂多价抑制作用。合成的纳米抑制剂可以在细胞外中和病毒粒子,并阻止其与宿主细胞的附着和进入。在存在反向设计的纳米抑制剂的情况下,病毒复制被显著降低了 6 个数量级。即使在感染后 24 小时使用,仍能实现超过 99.999%的抑制率,这表明这种纳米抑制剂可能是一种有效的抗流感病毒药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99cc/7497169/30c3efaed0a1/ANIE-59-15532-g001.jpg

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