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DC Field | Value | Language |
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dc.contributor.author | Baig, Mirza Saqib | en_US |
dc.contributor.author | Alagumuthu, Manikandan | en_US |
dc.contributor.author | Rajpoot, Sajjan | en_US |
dc.contributor.author | Saqib, Uzma | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-17T15:31:04Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-17T15:31:04Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Baig, M. S., Alagumuthu, M., Rajpoot, S., & Saqib, U. (2020). Identification of a potential peptide inhibitor of SARS-CoV-2 targeting its entry into the host cells. Drugs in R and D, 20(3), 161-169. doi:10.1007/s40268-020-00312-5 | en_US |
dc.identifier.issn | 1174-5886 | - |
dc.identifier.other | EID(2-s2.0-85087505447) | - |
dc.identifier.uri | https://doi.org/10.1007/s40268-020-00312-5 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/3934 | - |
dc.description.abstract | Background and objective: Coronavirus disease (COVID-19) is an ongoing pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Due to the incessant spread of the disease with substantial morbidity and mortality rates, there is an urgent demand for effective therapeutics and vaccines to control and diminish this pandemic. A critical step in the crosstalk between the virus and the host cell is the binding of SARS-CoV-2 spike protein to the angiotensin-converting enzyme 2 (ACE2) receptor present on the surface of the host cells. Hence, inhibition of this interaction could be a promising strategy to combat the SARS-CoV-2 infection. Methods: Docking and Molecular Dynamics (MD) simulation studies revealed that designed peptide maintains their secondary structure and provide a highly specific and stable binding (blocking) to SARS-CoV-2. Results: We have designed a novel peptide that could inhibit SARS-CoV-2 spike protein interaction with ACE2, thereby blocking the cellular entry of the virus. Conclusion: Our findings suggest that computationally developed inhibitory peptide may be developed as an anti-SARS-CoV-2 agent for the treatment of SARS-CoV-2 infection. We further plan to pursue the peptide in cell-based assays and eventually for clinical trials. © 2020, The Author(s). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Adis | en_US |
dc.source | Drugs in R and D | en_US |
dc.subject | angiotensin converting enzyme 2 | en_US |
dc.subject | anti-SARS-CoV-2 agent | en_US |
dc.subject | protein inhibitor | en_US |
dc.subject | viral protein | en_US |
dc.subject | angiotensin converting enzyme 2 | en_US |
dc.subject | antivirus agent | en_US |
dc.subject | coronavirus spike glycoprotein | en_US |
dc.subject | dipeptidyl carboxypeptidase | en_US |
dc.subject | peptide | en_US |
dc.subject | spike protein, SARS-CoV-2 | en_US |
dc.subject | virus vaccine | en_US |
dc.subject | Article | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug inhibition | en_US |
dc.subject | host cell | en_US |
dc.subject | molecular dynamics | en_US |
dc.subject | nonhuman | en_US |
dc.subject | physical chemistry | en_US |
dc.subject | priority journal | en_US |
dc.subject | protein protein interaction | en_US |
dc.subject | protein secondary structure | en_US |
dc.subject | Severe acute respiratory syndrome coronavirus 2 | en_US |
dc.subject | virus attachment | en_US |
dc.subject | virus entry | en_US |
dc.subject | virus spike | en_US |
dc.subject | Betacoronavirus | en_US |
dc.subject | Coronavirus infection | en_US |
dc.subject | human | en_US |
dc.subject | isolation and purification | en_US |
dc.subject | metabolism | en_US |
dc.subject | molecular docking | en_US |
dc.subject | pandemic | en_US |
dc.subject | virology | en_US |
dc.subject | virus pneumonia | en_US |
dc.subject | Antiviral Agents | en_US |
dc.subject | Betacoronavirus | en_US |
dc.subject | Coronavirus Infections | en_US |
dc.subject | Humans | en_US |
dc.subject | Molecular Docking Simulation | en_US |
dc.subject | Molecular Dynamics Simulation | en_US |
dc.subject | Pandemics | en_US |
dc.subject | Peptides | en_US |
dc.subject | Peptidyl-Dipeptidase A | en_US |
dc.subject | Pneumonia, Viral | en_US |
dc.subject | Spike Glycoprotein, Coronavirus | en_US |
dc.subject | Viral Vaccines | en_US |
dc.title | Identification of a Potential Peptide Inhibitor of SARS-CoV-2 Targeting its Entry into the Host Cells | en_US |
dc.type | Journal Article | en_US |
dc.rights.license | All Open Access, Gold, Green | - |
Appears in Collections: | Department of Biosciences and Biomedical Engineering |
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