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Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration

Herein, we have verified the interaction between the functional peptides from the SARS-CoV-2 and cell membrane, and we further proved that peptides exhibit little membrane disruption. The specific amino acids (Lys, Ile, Glu, Asn, Gln, etc.) with charge or hydrophobic residues play a significant role...

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Detalles Bibliográficos
Autores principales: Hao, Yun, Wu, Rongrong, Wang, Fenghua, Zhang, Liwei, Wang, Zengkai, Song, Xiaolu, Liu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179371/
https://www.ncbi.nlm.nih.gov/pubmed/35681433
http://dx.doi.org/10.3390/cells11111738
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author Hao, Yun
Wu, Rongrong
Wang, Fenghua
Zhang, Liwei
Wang, Zengkai
Song, Xiaolu
Liu, Lei
author_facet Hao, Yun
Wu, Rongrong
Wang, Fenghua
Zhang, Liwei
Wang, Zengkai
Song, Xiaolu
Liu, Lei
author_sort Hao, Yun
collection PubMed
description Herein, we have verified the interaction between the functional peptides from the SARS-CoV-2 and cell membrane, and we further proved that peptides exhibit little membrane disruption. The specific amino acids (Lys, Ile, Glu, Asn, Gln, etc.) with charge or hydrophobic residues play a significant role during the functional-peptide binding to membrane. The findings could provide the hints related to viral infection and also might pave the way for development of new materials based on peptides with membrane-binding activity, which would enable functional peptides further as peptide adjuvants, in order to help deliver the cancer drug into tumor cells for the efficient tumor therapy.
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spelling pubmed-91793712022-06-10 Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration Hao, Yun Wu, Rongrong Wang, Fenghua Zhang, Liwei Wang, Zengkai Song, Xiaolu Liu, Lei Cells Article Herein, we have verified the interaction between the functional peptides from the SARS-CoV-2 and cell membrane, and we further proved that peptides exhibit little membrane disruption. The specific amino acids (Lys, Ile, Glu, Asn, Gln, etc.) with charge or hydrophobic residues play a significant role during the functional-peptide binding to membrane. The findings could provide the hints related to viral infection and also might pave the way for development of new materials based on peptides with membrane-binding activity, which would enable functional peptides further as peptide adjuvants, in order to help deliver the cancer drug into tumor cells for the efficient tumor therapy. MDPI 2022-05-25 /pmc/articles/PMC9179371/ /pubmed/35681433 http://dx.doi.org/10.3390/cells11111738 Text en © 2022 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
Hao, Yun
Wu, Rongrong
Wang, Fenghua
Zhang, Liwei
Wang, Zengkai
Song, Xiaolu
Liu, Lei
Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title_full Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title_fullStr Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title_full_unstemmed Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title_short Functional Peptides from SARS-CoV-2 Binding with Cell Membrane: From Molecular Dynamics Simulations to Cell Demonstration
title_sort functional peptides from sars-cov-2 binding with cell membrane: from molecular dynamics simulations to cell demonstration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179371/
https://www.ncbi.nlm.nih.gov/pubmed/35681433
http://dx.doi.org/10.3390/cells11111738
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