病毒包膜
病毒进入
病毒结构蛋白
衣壳
病毒学
冠状病毒
病毒膜
生物
病毒蛋白
脂质双层融合
病毒复制
病毒
化学
2019年冠状病毒病(COVID-19)
传染病(医学专业)
医学
疾病
病理
作者
Hiroto Furukawa,Shoshiro Nakamura,Ryosuke Mizuta,Kentarou Sakamoto,Hiroshi Inaba,Shin‐ichi Sawada,Yoshihiro Sasaki,Kazunari Akiyoshi,Kazunori Matsuura
标识
DOI:10.1021/acssynbio.4c00165
摘要
Synthetic viral nanostructures are useful as materials for analyzing the biological behavior of natural viruses and as vaccine materials. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an enveloped virus embedding a spike (S) protein involved in host cell infection. Although nanomaterials modified with an S protein without an envelope membrane have been developed, they are considered unsuitable for stability and functionality. We previously constructed an enveloped viral replica complexed with a cationic lipid bilayer and an anionic artificial viral capsid self-assembled from β-annulus peptides. In this study, we report the first example of an enveloped viral replica equipped with an S protein derived from SARS-CoV-2. Interestingly, even the S protein equipped on the enveloped viral replica bound strongly to the free angiotensin-converting enzyme 2 (ACE2) receptor as well as ACE2 localized on the cell membrane.
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