Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustr. 3, 14195, Berlin, Germany.
Unit 17, Robert Koch Institut, Seestr. 10, 13353, Berlin, Germany.
Angew Chem Int Ed Engl. 2020 Sep 1;59(36):15532-15536. doi: 10.1002/anie.202004832. Epub 2020 Jul 8.
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.
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。