Please use this identifier to cite or link to this item:
https://dspace.iiti.ac.in/handle/123456789/3934
Title: | Identification of a Potential Peptide Inhibitor of SARS-CoV-2 Targeting its Entry into the Host Cells |
Authors: | Baig, Mirza Saqib Alagumuthu, Manikandan Rajpoot, Sajjan Saqib, Uzma |
Keywords: | angiotensin converting enzyme 2;anti-SARS-CoV-2 agent;protein inhibitor;viral protein;angiotensin converting enzyme 2;antivirus agent;coronavirus spike glycoprotein;dipeptidyl carboxypeptidase;peptide;spike protein, SARS-CoV-2;virus vaccine;Article;controlled study;drug inhibition;host cell;molecular dynamics;nonhuman;physical chemistry;priority journal;protein protein interaction;protein secondary structure;Severe acute respiratory syndrome coronavirus 2;virus attachment;virus entry;virus spike;Betacoronavirus;Coronavirus infection;human;isolation and purification;metabolism;molecular docking;pandemic;virology;virus pneumonia;Antiviral Agents;Betacoronavirus;Coronavirus Infections;Humans;Molecular Docking Simulation;Molecular Dynamics Simulation;Pandemics;Peptides;Peptidyl-Dipeptidase A;Pneumonia, Viral;Spike Glycoprotein, Coronavirus;Viral Vaccines |
Issue Date: | 2020 |
Publisher: | Adis |
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 |
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). |
URI: | https://doi.org/10.1007/s40268-020-00312-5 https://dspace.iiti.ac.in/handle/123456789/3934 |
ISSN: | 1174-5886 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Biosciences and Biomedical Engineering |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Altmetric Badge: