糖萼
脂质体
脂质双层融合
细胞膜
膜
生物物理学
病毒进入
冠状病毒
细胞
病毒
人工细胞
细胞生物学
病毒膜
化学
病毒包膜
生物
病毒学
生物化学
2019年冠状病毒病(COVID-19)
病毒复制
医学
疾病
病理
传染病(医学专业)
作者
Xu Li,Ningtao Cheng,Daqing Shi,Yutong Li,Chen Li,Miaojin Zhu,Qiao Jin,Zhigang Wu,Linwei Zhu,Yi He,Hang‐Ping Yao,Jian Ji
标识
DOI:10.1016/j.bioactmat.2023.10.021
摘要
As a broad-spectrum antiviral nanoparticle, the cell membrane nanodecoy is a promising strategy for preventing viral infections. However, most of the cell membrane nanodecoys can only catch virus and cannot induce inactivation, which may bring about a considerably high risk of re-infection owing to the possible viral escape from the nanodecoys. To tackle this challenge, sulfated liposomes are employed to mimic the cell membrane glycocalyx for constructing an artificial cell membrane glycocalyx nanodecoy that exhibits excellent anti-coronavirus activity against HCoV-OC43, wild-type SARS-CoV-2, Alpha and Delta variant SARS-CoV-2 pseudovirus. In addition, this nanodecoy, loaded with surface sulfate groups as SARS-CoV-2 receptor arrays, can enhance the antiviral capability to virus inactivation through destroying the virus membrane structure and transfer the spike protein to postfusion conformation. Integrating bio-inspired recognition and inactivation of viruses in a single supramolecular entity, the artificial cell membrane nanodecoy opens a new avenue for the development of theranostic antiviral nanosystems, whose mass production is favored due to the facile engineering of sulfated liposomes.
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