适体
病毒
DNA
俘获
化学
广谱
纳米技术
病毒学
生物物理学
细胞生物学
生物
组合化学
材料科学
分子生物学
生物化学
生态学
作者
Yunhua Guo,Wenzhe Song,Yuhang Dong,Xuejun Wang,Guangjun Nie,Feng Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-03-18
卷期号:24 (12): 3614-3623
被引量:6
标识
DOI:10.1021/acs.nanolett.3c04510
摘要
Broad-spectrum antiviral platforms are always desired but still lack the ability to cope with the threats to global public health. Herein, we develop a poly aptamer encoded DNA nanocatcher platform that can trap entire virus particles to inhibit infection with a broad antiviral spectrum. Ultralong single-stranded DNA (ssDNA) containing repeated aptamers was synthesized as the scaffold of a nanocatcher via a biocatalytic process, wherein mineralization of magnesium pyrophosphate on the ssDNA could occur and consequently lead to the formation of nanocatcher with interfacial nanocaves decorated with virus-binding aptamers. Once the viruses were recognized by the apatmers, they would be captured and trapped in the nanocaves via multisite synergistic interactions. Meanwhile, the size of nanocatchers was optimized to prevent their cellular uptake, which further guaranteed inhibition of virus infection. By taking SARS-CoV-2 variants as a model target, we demonstrated the broad virus-trapping capability of a DNA nanocatcher in engulfing the variants and blocking the infection to host cells.
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