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Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19
The recent emergence of different SARS-CoV-2 variants creates an urgent need to develop more effective therapeutic agents to prevent COVID-19 outbreaks. Among SARS-CoV-2 essential proteases is papain-like protease (SARS-CoV-2 PLpro), which plays multiple roles in regulating SARS-CoV-2 viral spread a...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Masson SAS.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106510/ https://www.ncbi.nlm.nih.gov/pubmed/37075625 http://dx.doi.org/10.1016/j.ejmech.2023.115380 |
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author | Hersi, Fatema Sebastian, Anusha Tarazi, Hamadeh Srinivasulu, Vunnam Mostafa, Ahmed Allayeh, Abdou Kamal Zeng, Cong Hachim, Ibrahim Y. Liu, Shan-Lu Abu-Yousef, Imad A. Majdalawieh, Amin F. Zaher, Dana M. Omar, Hany A. Al-Tel, Taleb H. |
author_facet | Hersi, Fatema Sebastian, Anusha Tarazi, Hamadeh Srinivasulu, Vunnam Mostafa, Ahmed Allayeh, Abdou Kamal Zeng, Cong Hachim, Ibrahim Y. Liu, Shan-Lu Abu-Yousef, Imad A. Majdalawieh, Amin F. Zaher, Dana M. Omar, Hany A. Al-Tel, Taleb H. |
author_sort | Hersi, Fatema |
collection | PubMed |
description | The recent emergence of different SARS-CoV-2 variants creates an urgent need to develop more effective therapeutic agents to prevent COVID-19 outbreaks. Among SARS-CoV-2 essential proteases is papain-like protease (SARS-CoV-2 PLpro), which plays multiple roles in regulating SARS-CoV-2 viral spread and innate immunity such as deubiquitinating and deISG15ylating (interferon-induced gene 15) activities. Many studies are currently focused on targeting this protease to tackle SARS-CoV-2 infection. In this context, we performed a phenotypic screening using an in-house pilot compounds collection possessing a diverse skeleta against SARS-CoV-2 PLpro. This screen identified SIMR3030 as a potent inhibitor of SARS-CoV-2. SIMR3030 has been shown to exhibit deubiquitinating activity and inhibition of SARS-CoV-2 specific gene expression (ORF1b and Spike) in infected host cells and possessing virucidal activity. Moreover, SIMR3030 was demonstrated to inhibit the expression of inflammatory markers, including IFN-α, IL-6, and OAS1, which are reported to mediate the development of cytokine storms and aggressive immune responses. In vitro absorption, distribution, metabolism, and excretion (ADME) assessment of the drug-likeness properties of SIMR3030 demonstrated good microsomal stability in liver microsomes. Furthermore, SIMR3030 demonstrated very low potency as an inhibitor of CYP450, CYP3A4, CYP2D6 and CYP2C9 which rules out any potential drug-drug interactions. In addition, SIMR3030 showed moderate permeability in Caco2-cells. Critically, SIMR3030 has maintained a high in vivo safety profile at different concentrations. Molecular modeling studies of SIMR3030 in the active sites of SARS-CoV-2 and MERS-CoV PLpro were performed to shed light on the binding modes of this inhibitor. This study demonstrates that SIMR3030 is a potent inhibitor of SARS-CoV-2 PLpro that forms the foundation for developing new drugs to tackle the COVID-19 pandemic and may pave the way for the development of novel therapeutics for a possible future outbreak of new SARS-CoV-2 variants or other Coronavirus species. |
format | Online Article Text |
id | pubmed-10106510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier Masson SAS. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101065102023-04-17 Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 Hersi, Fatema Sebastian, Anusha Tarazi, Hamadeh Srinivasulu, Vunnam Mostafa, Ahmed Allayeh, Abdou Kamal Zeng, Cong Hachim, Ibrahim Y. Liu, Shan-Lu Abu-Yousef, Imad A. Majdalawieh, Amin F. Zaher, Dana M. Omar, Hany A. Al-Tel, Taleb H. Eur J Med Chem Research Paper The recent emergence of different SARS-CoV-2 variants creates an urgent need to develop more effective therapeutic agents to prevent COVID-19 outbreaks. Among SARS-CoV-2 essential proteases is papain-like protease (SARS-CoV-2 PLpro), which plays multiple roles in regulating SARS-CoV-2 viral spread and innate immunity such as deubiquitinating and deISG15ylating (interferon-induced gene 15) activities. Many studies are currently focused on targeting this protease to tackle SARS-CoV-2 infection. In this context, we performed a phenotypic screening using an in-house pilot compounds collection possessing a diverse skeleta against SARS-CoV-2 PLpro. This screen identified SIMR3030 as a potent inhibitor of SARS-CoV-2. SIMR3030 has been shown to exhibit deubiquitinating activity and inhibition of SARS-CoV-2 specific gene expression (ORF1b and Spike) in infected host cells and possessing virucidal activity. Moreover, SIMR3030 was demonstrated to inhibit the expression of inflammatory markers, including IFN-α, IL-6, and OAS1, which are reported to mediate the development of cytokine storms and aggressive immune responses. In vitro absorption, distribution, metabolism, and excretion (ADME) assessment of the drug-likeness properties of SIMR3030 demonstrated good microsomal stability in liver microsomes. Furthermore, SIMR3030 demonstrated very low potency as an inhibitor of CYP450, CYP3A4, CYP2D6 and CYP2C9 which rules out any potential drug-drug interactions. In addition, SIMR3030 showed moderate permeability in Caco2-cells. Critically, SIMR3030 has maintained a high in vivo safety profile at different concentrations. Molecular modeling studies of SIMR3030 in the active sites of SARS-CoV-2 and MERS-CoV PLpro were performed to shed light on the binding modes of this inhibitor. This study demonstrates that SIMR3030 is a potent inhibitor of SARS-CoV-2 PLpro that forms the foundation for developing new drugs to tackle the COVID-19 pandemic and may pave the way for the development of novel therapeutics for a possible future outbreak of new SARS-CoV-2 variants or other Coronavirus species. Elsevier Masson SAS. 2023-06-05 2023-04-17 /pmc/articles/PMC10106510/ /pubmed/37075625 http://dx.doi.org/10.1016/j.ejmech.2023.115380 Text en © 2023 Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Research Paper Hersi, Fatema Sebastian, Anusha Tarazi, Hamadeh Srinivasulu, Vunnam Mostafa, Ahmed Allayeh, Abdou Kamal Zeng, Cong Hachim, Ibrahim Y. Liu, Shan-Lu Abu-Yousef, Imad A. Majdalawieh, Amin F. Zaher, Dana M. Omar, Hany A. Al-Tel, Taleb H. Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title | Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title_full | Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title_fullStr | Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title_full_unstemmed | Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title_short | Discovery of novel papain-like protease inhibitors for potential treatment of COVID-19 |
title_sort | discovery of novel papain-like protease inhibitors for potential treatment of covid-19 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106510/ https://www.ncbi.nlm.nih.gov/pubmed/37075625 http://dx.doi.org/10.1016/j.ejmech.2023.115380 |
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