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Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach

Vibrio cholerae causes the diarrheal disease cholera which affects millions of people globally. The outer membrane protein U (OmpU) is the outer membrane protein that is most prevalent in V. cholerae and has already been recognized as a critical component of pathogenicity involved in host cell conta...

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Autores principales: Rahaman, Abdul, Almalki, Abdulraheem Ali, Rafeeq, Misbahuddin M., Akhtar, Omar, Anjum, Farah, Mashraqi, Mutaib M., Sain, Ziaullah M., Alzamami, Ahmad, Ahmad, Varish, Zeng, Xin-An, Jamal, Qazi Mohammad Sajid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588037/
https://www.ncbi.nlm.nih.gov/pubmed/34770925
http://dx.doi.org/10.3390/molecules26216517
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author Rahaman, Abdul
Almalki, Abdulraheem Ali
Rafeeq, Misbahuddin M.
Akhtar, Omar
Anjum, Farah
Mashraqi, Mutaib M.
Sain, Ziaullah M.
Alzamami, Ahmad
Ahmad, Varish
Zeng, Xin-An
Jamal, Qazi Mohammad Sajid
author_facet Rahaman, Abdul
Almalki, Abdulraheem Ali
Rafeeq, Misbahuddin M.
Akhtar, Omar
Anjum, Farah
Mashraqi, Mutaib M.
Sain, Ziaullah M.
Alzamami, Ahmad
Ahmad, Varish
Zeng, Xin-An
Jamal, Qazi Mohammad Sajid
author_sort Rahaman, Abdul
collection PubMed
description Vibrio cholerae causes the diarrheal disease cholera which affects millions of people globally. The outer membrane protein U (OmpU) is the outer membrane protein that is most prevalent in V. cholerae and has already been recognized as a critical component of pathogenicity involved in host cell contact and as being necessary for the survival of pathogenic V. cholerae in the host body. Computational approaches were used in this study to screen a total of 37,709 natural compounds from the traditional Chinese medicine (TCM) database against the active site of OmpU. Following a sequential screening of the TCM database, we report three lead compounds—ZINC06494587, ZINC85510056, and ZINC95910434—that bind strongly to OmpU, with binding affinity values of −8.92, −8.12, and −8.78 kcal/mol, which were higher than the control ligand (−7.0 kcal/mol). To optimize the interaction, several 100 ns molecular dynamics simulations were performed, and the resulting complexes were shown to be stable in their vicinity. Additionally, these compounds were predicted to have good drug-like properties based on physicochemical properties and ADMET assessments. This study suggests that further research be conducted on these compounds to determine their potential use as cholera disease treatment.
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spelling pubmed-85880372021-11-13 Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach Rahaman, Abdul Almalki, Abdulraheem Ali Rafeeq, Misbahuddin M. Akhtar, Omar Anjum, Farah Mashraqi, Mutaib M. Sain, Ziaullah M. Alzamami, Ahmad Ahmad, Varish Zeng, Xin-An Jamal, Qazi Mohammad Sajid Molecules Article Vibrio cholerae causes the diarrheal disease cholera which affects millions of people globally. The outer membrane protein U (OmpU) is the outer membrane protein that is most prevalent in V. cholerae and has already been recognized as a critical component of pathogenicity involved in host cell contact and as being necessary for the survival of pathogenic V. cholerae in the host body. Computational approaches were used in this study to screen a total of 37,709 natural compounds from the traditional Chinese medicine (TCM) database against the active site of OmpU. Following a sequential screening of the TCM database, we report three lead compounds—ZINC06494587, ZINC85510056, and ZINC95910434—that bind strongly to OmpU, with binding affinity values of −8.92, −8.12, and −8.78 kcal/mol, which were higher than the control ligand (−7.0 kcal/mol). To optimize the interaction, several 100 ns molecular dynamics simulations were performed, and the resulting complexes were shown to be stable in their vicinity. Additionally, these compounds were predicted to have good drug-like properties based on physicochemical properties and ADMET assessments. This study suggests that further research be conducted on these compounds to determine their potential use as cholera disease treatment. MDPI 2021-10-28 /pmc/articles/PMC8588037/ /pubmed/34770925 http://dx.doi.org/10.3390/molecules26216517 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rahaman, Abdul
Almalki, Abdulraheem Ali
Rafeeq, Misbahuddin M.
Akhtar, Omar
Anjum, Farah
Mashraqi, Mutaib M.
Sain, Ziaullah M.
Alzamami, Ahmad
Ahmad, Varish
Zeng, Xin-An
Jamal, Qazi Mohammad Sajid
Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title_full Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title_fullStr Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title_full_unstemmed Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title_short Identification of Potent Natural Resource Small Molecule Inhibitor to Control Vibrio cholera by Targeting Its Outer Membrane Protein U: An In Silico Approach
title_sort identification of potent natural resource small molecule inhibitor to control vibrio cholera by targeting its outer membrane protein u: an in silico approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588037/
https://www.ncbi.nlm.nih.gov/pubmed/34770925
http://dx.doi.org/10.3390/molecules26216517
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