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Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa

It is well established fact that peptides from various foods offer human health benefits displaying diverse functionalities. Millets considered as super foods is a major alternative in recent days for traditional diet being rich in proteins and fibre along with trace minerals and vitamins. In this c...

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Autores principales: Rangaswamy, Ashok Nanjaiah, Ashok, Arpitha, Hanumanthappa, Pradeep, Chandrashekaramurthy, Aparanji Sinduvalli, Kumbaiah, Monika, Hiregouda, Pratibha, Sharma, Vaishali, Sosalegowda, Aparna Huligerepura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8030649/
https://www.ncbi.nlm.nih.gov/pubmed/33850482
http://dx.doi.org/10.1007/s10989-021-10211-1
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author Rangaswamy, Ashok Nanjaiah
Ashok, Arpitha
Hanumanthappa, Pradeep
Chandrashekaramurthy, Aparanji Sinduvalli
Kumbaiah, Monika
Hiregouda, Pratibha
Sharma, Vaishali
Sosalegowda, Aparna Huligerepura
author_facet Rangaswamy, Ashok Nanjaiah
Ashok, Arpitha
Hanumanthappa, Pradeep
Chandrashekaramurthy, Aparanji Sinduvalli
Kumbaiah, Monika
Hiregouda, Pratibha
Sharma, Vaishali
Sosalegowda, Aparna Huligerepura
author_sort Rangaswamy, Ashok Nanjaiah
collection PubMed
description It is well established fact that peptides from various foods offer human health benefits displaying diverse functionalities. Millets considered as super foods is a major alternative in recent days for traditional diet being rich in proteins and fibre along with trace minerals and vitamins. In this connection, proteins from Buckwheat and Quinoa were digested by in vitro simulation digestion for the generation of peptides, analyzed by nLC-MS/MS and the functional annotations of the identified proteins/peptides were carried out. The study led to the identification of 34 small peptides and their parent proteins clustered into 4 gene functional groups and their localization prediction indicated their involvement in energy metabolism, transport and storage. Interestingly, the identified peptides maximally displayed DPP-IV and ACE inhibitions. The present study was extended to unravel ACE-2 inhibition targeting COVID-19 by selecting ACE-2-Spike binding domain for molecular docking studies. The NWRTVKYG interacted with the ACE-2-Spike interface displaying the feasible binding energy (− 213.63) and docking score (− 12.43) and the MD simulation revealed the ability of the peptide in stabilizing the protein-peptide composite. The present investigation thus establishes newer vista for food derived peptides having ACE-2 inhibitory potential as tentative strategy for SARS-CoV-2 therapeutics.
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spelling pubmed-80306492021-04-09 Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa Rangaswamy, Ashok Nanjaiah Ashok, Arpitha Hanumanthappa, Pradeep Chandrashekaramurthy, Aparanji Sinduvalli Kumbaiah, Monika Hiregouda, Pratibha Sharma, Vaishali Sosalegowda, Aparna Huligerepura Int J Pept Res Ther Article It is well established fact that peptides from various foods offer human health benefits displaying diverse functionalities. Millets considered as super foods is a major alternative in recent days for traditional diet being rich in proteins and fibre along with trace minerals and vitamins. In this connection, proteins from Buckwheat and Quinoa were digested by in vitro simulation digestion for the generation of peptides, analyzed by nLC-MS/MS and the functional annotations of the identified proteins/peptides were carried out. The study led to the identification of 34 small peptides and their parent proteins clustered into 4 gene functional groups and their localization prediction indicated their involvement in energy metabolism, transport and storage. Interestingly, the identified peptides maximally displayed DPP-IV and ACE inhibitions. The present study was extended to unravel ACE-2 inhibition targeting COVID-19 by selecting ACE-2-Spike binding domain for molecular docking studies. The NWRTVKYG interacted with the ACE-2-Spike interface displaying the feasible binding energy (− 213.63) and docking score (− 12.43) and the MD simulation revealed the ability of the peptide in stabilizing the protein-peptide composite. The present investigation thus establishes newer vista for food derived peptides having ACE-2 inhibitory potential as tentative strategy for SARS-CoV-2 therapeutics. Springer Netherlands 2021-04-08 2021 /pmc/articles/PMC8030649/ /pubmed/33850482 http://dx.doi.org/10.1007/s10989-021-10211-1 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Rangaswamy, Ashok Nanjaiah
Ashok, Arpitha
Hanumanthappa, Pradeep
Chandrashekaramurthy, Aparanji Sinduvalli
Kumbaiah, Monika
Hiregouda, Pratibha
Sharma, Vaishali
Sosalegowda, Aparna Huligerepura
Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title_full Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title_fullStr Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title_full_unstemmed Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title_short Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa
title_sort identification of potential peptide inhibitors of ace-2 target of sars-cov-2 from buckwheat & quinoa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8030649/
https://www.ncbi.nlm.nih.gov/pubmed/33850482
http://dx.doi.org/10.1007/s10989-021-10211-1
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