Enveloped Viral Replica Equipped with Spike Protein Derived from SARS-CoV-2
Hiroto Furukawa, Sosuke Nakamura, Ryosuke Mizuta, Kentarou Sakamoto, Hiroshi Inaba, Shin‐ichi Sawada, Yoshihiro Sasaki, Kazunari Akiyoshi, Kazunori Matsuura
Abstract
Hiroto Furukawa, Sosuke Nakamura, Ryosuke Mizuta, Kentarou Sakamoto, Hiroshi Inaba, Shin‐ichi Sawada, Yoshihiro Sasaki, Kazunari Akiyoshi, Kazunori Matsuura
Abstract
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.
OpenAlex reports 9 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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.
Key concepts: Spike (software development), Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Virology, Spike Protein, Replica, 2019-20 coronavirus outbreak, Coronavirus disease 2019 (COVID-19), Biology