Cargando…

3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor

The global spread of the novel coronavirus SARS-CoV-2 urgently requires discovery of effective therapeutics for the treatment of COVID-19. The spike (S) protein of SARS-CoV-2 plays a key role in receptor recognition, virus-cell membrane fusion and virus entry. Our previous studies have reported that...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Taizhen, Qiu, Jiayin, Niu, Xiaoge, Ma, Qinhai, Zhou, Chenliang, Chen, Pei, Zhang, Qiao, Chen, Meiyun, Yang, Zifeng, Liu, Shuwen, Li, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840605/
https://www.ncbi.nlm.nih.gov/pubmed/33519467
http://dx.doi.org/10.3389/fphar.2020.603830
_version_ 1783643614025351168
author Liang, Taizhen
Qiu, Jiayin
Niu, Xiaoge
Ma, Qinhai
Zhou, Chenliang
Chen, Pei
Zhang, Qiao
Chen, Meiyun
Yang, Zifeng
Liu, Shuwen
Li, Lin
author_facet Liang, Taizhen
Qiu, Jiayin
Niu, Xiaoge
Ma, Qinhai
Zhou, Chenliang
Chen, Pei
Zhang, Qiao
Chen, Meiyun
Yang, Zifeng
Liu, Shuwen
Li, Lin
author_sort Liang, Taizhen
collection PubMed
description The global spread of the novel coronavirus SARS-CoV-2 urgently requires discovery of effective therapeutics for the treatment of COVID-19. The spike (S) protein of SARS-CoV-2 plays a key role in receptor recognition, virus-cell membrane fusion and virus entry. Our previous studies have reported that 3-hydroxyphthalic anhydride-modified chicken ovalbumin (HP-OVA) serves as a viral entry inhibitor to prevent several kinds of virus infection. Here, our results reveal that HP-OVA can effectively inhibit SARS-CoV-2 replication and S protein-mediated cell-cell fusion in a dose-dependent manner without obvious cytopathic effects. Further analysis suggests that HP-OVA can bind to both the S protein of SARS-CoV-2 and host angiotensin-converting enzyme 2 (ACE2), the functional receptor of SARS-CoV-2, and disrupt the S protein-ACE2 interaction, thereby exhibiting inhibitory activity against SARS-CoV-2 infection. In summary, our findings suggest that HP-OVA can serve as a potential therapeutic agent for the treatment of deadly COVID-19.
format Online
Article
Text
id pubmed-7840605
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-78406052021-01-29 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor Liang, Taizhen Qiu, Jiayin Niu, Xiaoge Ma, Qinhai Zhou, Chenliang Chen, Pei Zhang, Qiao Chen, Meiyun Yang, Zifeng Liu, Shuwen Li, Lin Front Pharmacol Pharmacology The global spread of the novel coronavirus SARS-CoV-2 urgently requires discovery of effective therapeutics for the treatment of COVID-19. The spike (S) protein of SARS-CoV-2 plays a key role in receptor recognition, virus-cell membrane fusion and virus entry. Our previous studies have reported that 3-hydroxyphthalic anhydride-modified chicken ovalbumin (HP-OVA) serves as a viral entry inhibitor to prevent several kinds of virus infection. Here, our results reveal that HP-OVA can effectively inhibit SARS-CoV-2 replication and S protein-mediated cell-cell fusion in a dose-dependent manner without obvious cytopathic effects. Further analysis suggests that HP-OVA can bind to both the S protein of SARS-CoV-2 and host angiotensin-converting enzyme 2 (ACE2), the functional receptor of SARS-CoV-2, and disrupt the S protein-ACE2 interaction, thereby exhibiting inhibitory activity against SARS-CoV-2 infection. In summary, our findings suggest that HP-OVA can serve as a potential therapeutic agent for the treatment of deadly COVID-19. Frontiers Media S.A. 2021-01-14 /pmc/articles/PMC7840605/ /pubmed/33519467 http://dx.doi.org/10.3389/fphar.2020.603830 Text en Copyright © 2021 Liang, Qiu, Niu, Ma, Zhou, Chen, Zhang, Chen, Yang, Liu and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Liang, Taizhen
Qiu, Jiayin
Niu, Xiaoge
Ma, Qinhai
Zhou, Chenliang
Chen, Pei
Zhang, Qiao
Chen, Meiyun
Yang, Zifeng
Liu, Shuwen
Li, Lin
3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title_full 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title_fullStr 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title_full_unstemmed 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title_short 3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor
title_sort 3-hydroxyphthalic anhydride-modified chicken ovalbumin as a potential candidate inhibits sars-cov-2 infection by disrupting the interaction of spike protein with host ace2 receptor
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840605/
https://www.ncbi.nlm.nih.gov/pubmed/33519467
http://dx.doi.org/10.3389/fphar.2020.603830
work_keys_str_mv AT liangtaizhen 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT qiujiayin 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT niuxiaoge 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT maqinhai 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT zhouchenliang 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT chenpei 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT zhangqiao 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT chenmeiyun 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT yangzifeng 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT liushuwen 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor
AT lilin 3hydroxyphthalicanhydridemodifiedchickenovalbuminasapotentialcandidateinhibitssarscov2infectionbydisruptingtheinteractionofspikeproteinwithhostace2receptor