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Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition
Furin is a potential target protein associated with numerous diseases; especially closely related to tumors and multiple viral infections including SARS-CoV-2. Most of the existing efficient furin inhibitors adopt a substrate analogous structure, and other types of small molecule inhibitors need to...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959265/ https://www.ncbi.nlm.nih.gov/pubmed/36838867 http://dx.doi.org/10.3390/molecules28041883 |
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author | Feng, Dongyan Ren, Le Wu, Jiaqi Guo, Lingling Han, Zhitao Yang, Jingjing Xie, Wei Wang, Yanbing Xu, Fanxing Su, Xin Li, Dahong Cao, Hao |
author_facet | Feng, Dongyan Ren, Le Wu, Jiaqi Guo, Lingling Han, Zhitao Yang, Jingjing Xie, Wei Wang, Yanbing Xu, Fanxing Su, Xin Li, Dahong Cao, Hao |
author_sort | Feng, Dongyan |
collection | PubMed |
description | Furin is a potential target protein associated with numerous diseases; especially closely related to tumors and multiple viral infections including SARS-CoV-2. Most of the existing efficient furin inhibitors adopt a substrate analogous structure, and other types of small molecule inhibitors need to be discovered urgently. In this study, a high-throughput screening combining virtual and physical screening of natural product libraries was performed, coupled with experimental validation and preliminary mechanistic assays at the molecular level, cellular level, and molecular simulation. A novel furin inhibitor, permethrin, which is a derivative from pyrethrin I generated by Pyrethrum cinerariifolium Trev. was identified, and this study confirmed that it binds to a novel allosteric pocket of furin through non-competitive inhibition. It exhibits a very favorable protease-selective inhibition and good cellular activity and specificity. In summary, permethrin shows a new parent nucleus with a new mode of inhibition. It could be used as a highly promising lead compound against furin for targeting related tumors and various resistant viral infections, including SARS-CoV-2. |
format | Online Article Text |
id | pubmed-9959265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99592652023-02-26 Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition Feng, Dongyan Ren, Le Wu, Jiaqi Guo, Lingling Han, Zhitao Yang, Jingjing Xie, Wei Wang, Yanbing Xu, Fanxing Su, Xin Li, Dahong Cao, Hao Molecules Communication Furin is a potential target protein associated with numerous diseases; especially closely related to tumors and multiple viral infections including SARS-CoV-2. Most of the existing efficient furin inhibitors adopt a substrate analogous structure, and other types of small molecule inhibitors need to be discovered urgently. In this study, a high-throughput screening combining virtual and physical screening of natural product libraries was performed, coupled with experimental validation and preliminary mechanistic assays at the molecular level, cellular level, and molecular simulation. A novel furin inhibitor, permethrin, which is a derivative from pyrethrin I generated by Pyrethrum cinerariifolium Trev. was identified, and this study confirmed that it binds to a novel allosteric pocket of furin through non-competitive inhibition. It exhibits a very favorable protease-selective inhibition and good cellular activity and specificity. In summary, permethrin shows a new parent nucleus with a new mode of inhibition. It could be used as a highly promising lead compound against furin for targeting related tumors and various resistant viral infections, including SARS-CoV-2. MDPI 2023-02-16 /pmc/articles/PMC9959265/ /pubmed/36838867 http://dx.doi.org/10.3390/molecules28041883 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Feng, Dongyan Ren, Le Wu, Jiaqi Guo, Lingling Han, Zhitao Yang, Jingjing Xie, Wei Wang, Yanbing Xu, Fanxing Su, Xin Li, Dahong Cao, Hao Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title | Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title_full | Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title_fullStr | Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title_full_unstemmed | Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title_short | Permethrin as a Potential Furin Inhibitor through a Novel Non-Competitive Allosteric Inhibition |
title_sort | permethrin as a potential furin inhibitor through a novel non-competitive allosteric inhibition |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959265/ https://www.ncbi.nlm.nih.gov/pubmed/36838867 http://dx.doi.org/10.3390/molecules28041883 |
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