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Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria

The medical application of chitosan (Cs) has been for about half a century, but the molecular mechanism has not been elucidated yet. This study is to explore the antibacterial mechanism of chitosan nanoparticles (Csnp) in dentin at the atomic resolution level. Extracted tooth specimen was prepared i...

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Autores principales: Zhou, Ziliang, Yang, Yanyan, He, Lu, Wang, Junmei, Xiong, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106623/
https://www.ncbi.nlm.nih.gov/pubmed/35551510
http://dx.doi.org/10.1007/s10856-022-06665-4
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author Zhou, Ziliang
Yang, Yanyan
He, Lu
Wang, Junmei
Xiong, Jie
author_facet Zhou, Ziliang
Yang, Yanyan
He, Lu
Wang, Junmei
Xiong, Jie
author_sort Zhou, Ziliang
collection PubMed
description The medical application of chitosan (Cs) has been for about half a century, but the molecular mechanism has not been elucidated yet. This study is to explore the antibacterial mechanism of chitosan nanoparticles (Csnp) in dentin at the atomic resolution level. Extracted tooth specimen was prepared in three groups: A. control group; B. Csnp treatment under ultrasonic agitation (UA); C. Csnp treatment without UA. A scanning electron microscope (SEM) was used to observe the Csnp distribution on the dentin surface. The incubations of Enterococcus faecalis (E. faecalis) were performed. Further, we explored the protection mechanism of chitosan polymers to collagen type I, using molecular docking technique and crystal structure superimposition analysis. We revealed that Csnp under UA was evenly distributed on the dental surface and the Csnp-pretreated dentin had great antibacterial activity for E. faecalis. Our work demonstrated that Csnp occupied the grooves of the triple-helical collagen surface, strengthened by crosslinking, and interfered with the bond of collagen adhesin through steric hindrance effect and interrupting hydrophobic interaction. Csnp protects dentin against E. faecalis by interacting and crosslinking with collagen type I and prevents bacterial collagen adhesin binding through steric hindrance effect and interrupting hydrophobic interaction. [Figure: see text]
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spelling pubmed-91066232022-05-15 Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria Zhou, Ziliang Yang, Yanyan He, Lu Wang, Junmei Xiong, Jie J Mater Sci Mater Med Biomaterials Synthesis and Characterization The medical application of chitosan (Cs) has been for about half a century, but the molecular mechanism has not been elucidated yet. This study is to explore the antibacterial mechanism of chitosan nanoparticles (Csnp) in dentin at the atomic resolution level. Extracted tooth specimen was prepared in three groups: A. control group; B. Csnp treatment under ultrasonic agitation (UA); C. Csnp treatment without UA. A scanning electron microscope (SEM) was used to observe the Csnp distribution on the dentin surface. The incubations of Enterococcus faecalis (E. faecalis) were performed. Further, we explored the protection mechanism of chitosan polymers to collagen type I, using molecular docking technique and crystal structure superimposition analysis. We revealed that Csnp under UA was evenly distributed on the dental surface and the Csnp-pretreated dentin had great antibacterial activity for E. faecalis. Our work demonstrated that Csnp occupied the grooves of the triple-helical collagen surface, strengthened by crosslinking, and interfered with the bond of collagen adhesin through steric hindrance effect and interrupting hydrophobic interaction. Csnp protects dentin against E. faecalis by interacting and crosslinking with collagen type I and prevents bacterial collagen adhesin binding through steric hindrance effect and interrupting hydrophobic interaction. [Figure: see text] Springer US 2022-05-13 2022 /pmc/articles/PMC9106623/ /pubmed/35551510 http://dx.doi.org/10.1007/s10856-022-06665-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biomaterials Synthesis and Characterization
Zhou, Ziliang
Yang, Yanyan
He, Lu
Wang, Junmei
Xiong, Jie
Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title_full Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title_fullStr Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title_full_unstemmed Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title_short Molecular docking reveals Chitosan nanoparticle protection mechanism for dentin against Collagen-binding bacteria
title_sort molecular docking reveals chitosan nanoparticle protection mechanism for dentin against collagen-binding bacteria
topic Biomaterials Synthesis and Characterization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106623/
https://www.ncbi.nlm.nih.gov/pubmed/35551510
http://dx.doi.org/10.1007/s10856-022-06665-4
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