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Structure-based virtual screening methods for the identification of novel phytochemical inhibitors targeting furin protease for the management of COVID-19.
- Source :
-
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2024 Jun 11; Vol. 14, pp. 1391288. Date of Electronic Publication: 2024 Jun 11 (Print Publication: 2024). - Publication Year :
- 2024
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Abstract
- The coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, is a highly contagious respiratory disease with widespread societal impact. The symptoms range from cough, fever, and pneumonia to complications affecting various organs, including the heart, kidneys, and nervous system. Despite various ongoing efforts, no effective drug has been developed to stop the spread of the virus. Although various types of medications used to treat bacterial and viral diseases have previously been employed to treat COVID-19 patients, their side effects have also been observed. The way SARS-CoV-2 infects the human body is very specific, as its spike protein plays an important role. The S subunit of virus spike protein cleaved by human proteases, such as furin protein, is an initial and important step for its internalization into a human host. Keeping this context, we attempted to inhibit the furin using phytochemicals that could produce minimal side effects. For this, we screened 408 natural phytochemicals from various plants having antiviral properties, against furin protein, and molecular docking and dynamics simulations were performed. Based on the binding score, the top three compounds (robustaflavone, withanolide, and amentoflavone) were selected for further validation. MM/GBSA energy calculations revealed that withanolide has the lowest binding energy of -57.2 kcal/mol followed by robustaflavone and amentoflavone with a binding energy of -45.2 kcal/mol and -39.68 kcal/mol, respectively. Additionally, ADME analysis showed drug-like properties for these three lead compounds. Hence, these natural compounds robustaflavone, withanolide, and amentoflavone, may have therapeutic potential for the management of SARS-CoV-2 by targeting furin.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Kumar Tiwari, Chouhan, Mishra, Gupta, Chaudhary, Al-Zharani, Ahmed Qurtam, Nasr, Jha, Pant, Kumar and Kumar.)
- Subjects :
- Humans
Protease Inhibitors pharmacology
Protease Inhibitors chemistry
Spike Glycoprotein, Coronavirus metabolism
Spike Glycoprotein, Coronavirus antagonists & inhibitors
Spike Glycoprotein, Coronavirus chemistry
COVID-19 virology
Protein Binding
Furin antagonists & inhibitors
Furin metabolism
Phytochemicals pharmacology
Phytochemicals chemistry
Molecular Docking Simulation
SARS-CoV-2 drug effects
SARS-CoV-2 enzymology
Antiviral Agents pharmacology
Antiviral Agents chemistry
COVID-19 Drug Treatment
Subjects
Details
- Language :
- English
- ISSN :
- 2235-2988
- Volume :
- 14
- Database :
- MEDLINE
- Journal :
- Frontiers in cellular and infection microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 38919703
- Full Text :
- https://doi.org/10.3389/fcimb.2024.1391288