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Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19
SARS-CoV-2 is a positive-sense RNA virus and it is the causative agent of the global COVID-19 outbreak. COVID-19 is similar to the previous outbreaks for instance SARS in 2002-2003 and MERS in 2012. As the peptides have many advantages, peptide-based therapeutics might be one of the possible ways in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498005/ https://www.ncbi.nlm.nih.gov/pubmed/34689960 http://dx.doi.org/10.1016/j.therap.2021.09.007 |
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author | Shah, Jagat Narayan Guo, Guang-Qin Krishnan, Anand Ramesh, Muthusamy Katari, Naresh Kumar Shahbaaz, Mohd Abdellattif, Magda H. Singh, Sachin Kumar Dua, Kamal |
author_facet | Shah, Jagat Narayan Guo, Guang-Qin Krishnan, Anand Ramesh, Muthusamy Katari, Naresh Kumar Shahbaaz, Mohd Abdellattif, Magda H. Singh, Sachin Kumar Dua, Kamal |
author_sort | Shah, Jagat Narayan |
collection | PubMed |
description | SARS-CoV-2 is a positive-sense RNA virus and it is the causative agent of the global COVID-19 outbreak. COVID-19 is similar to the previous outbreaks for instance SARS in 2002-2003 and MERS in 2012. As the peptides have many advantages, peptide-based therapeutics might be one of the possible ways in the development of COVID-19 specific drugs. SARS-CoV-2 enters into a human via its S protein by attaching with human hACE2 present on the cell membrane in the lungs and intestines of humans. hACE2 cleaves S protein into the S1 subunit for viral attachment and the S2 subunit for fusion with the host cell membrane. The fusion mechanism forms a six-helical bundle (6-HB) structure which finally fuses the viral envelope with the host cell membrane. hACE2 based peptides such as SBP1 and Spikeplug have shown their potential as antiviral agents. S protein-hACE2 interaction and the SARS-CoV-2 fusion machinery play a crucial part in human viral infection. It is evident that if these interactions could be blocked successfully and efficiently, it could be the way to find the drug for COVID-19. Several peptide-based inhibitors are potent inhibitors of S protein-hACE2 interaction. Similarly, the antiviral activity of the antimicrobial peptide, lactoferrin makes it an important candidate for the COVID-19 drug development process. A candidate drug, RhACE2-APN01 based on recombinant hACE2 peptide has already entered phase II clinical trials. This review sheds light on different aspects of the feasibility of using peptide-based therapeutics as the promising therapeutic route for COVID-19. |
format | Online Article Text |
id | pubmed-8498005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84980052021-10-08 Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 Shah, Jagat Narayan Guo, Guang-Qin Krishnan, Anand Ramesh, Muthusamy Katari, Naresh Kumar Shahbaaz, Mohd Abdellattif, Magda H. Singh, Sachin Kumar Dua, Kamal Therapie Clinical Pharmacology SARS-CoV-2 is a positive-sense RNA virus and it is the causative agent of the global COVID-19 outbreak. COVID-19 is similar to the previous outbreaks for instance SARS in 2002-2003 and MERS in 2012. As the peptides have many advantages, peptide-based therapeutics might be one of the possible ways in the development of COVID-19 specific drugs. SARS-CoV-2 enters into a human via its S protein by attaching with human hACE2 present on the cell membrane in the lungs and intestines of humans. hACE2 cleaves S protein into the S1 subunit for viral attachment and the S2 subunit for fusion with the host cell membrane. The fusion mechanism forms a six-helical bundle (6-HB) structure which finally fuses the viral envelope with the host cell membrane. hACE2 based peptides such as SBP1 and Spikeplug have shown their potential as antiviral agents. S protein-hACE2 interaction and the SARS-CoV-2 fusion machinery play a crucial part in human viral infection. It is evident that if these interactions could be blocked successfully and efficiently, it could be the way to find the drug for COVID-19. Several peptide-based inhibitors are potent inhibitors of S protein-hACE2 interaction. Similarly, the antiviral activity of the antimicrobial peptide, lactoferrin makes it an important candidate for the COVID-19 drug development process. A candidate drug, RhACE2-APN01 based on recombinant hACE2 peptide has already entered phase II clinical trials. This review sheds light on different aspects of the feasibility of using peptide-based therapeutics as the promising therapeutic route for COVID-19. Société française de pharmacologie et de thérapeutique. Published by Elsevier Masson SAS. 2022 2021-10-08 /pmc/articles/PMC8498005/ /pubmed/34689960 http://dx.doi.org/10.1016/j.therap.2021.09.007 Text en © 2021 Société française de pharmacologie et de thérapeutique. Published by 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 | Clinical Pharmacology Shah, Jagat Narayan Guo, Guang-Qin Krishnan, Anand Ramesh, Muthusamy Katari, Naresh Kumar Shahbaaz, Mohd Abdellattif, Magda H. Singh, Sachin Kumar Dua, Kamal Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title | Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title_full | Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title_fullStr | Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title_full_unstemmed | Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title_short | Peptides-based therapeutics: Emerging potential therapeutic agents for COVID-19 |
title_sort | peptides-based therapeutics: emerging potential therapeutic agents for covid-19 |
topic | Clinical Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498005/ https://www.ncbi.nlm.nih.gov/pubmed/34689960 http://dx.doi.org/10.1016/j.therap.2021.09.007 |
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