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Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis

BACKGROUND: As an emerging research area of artificial enzymes, nanozyme, the catalytic nanomaterials with enzyme-like characteristics, have attracted enormous attention in research. Here, a nanozyme probe has been realized by utilizing antigen-labeled mesoporous silica-encapsulated Au-core Pt-shell...

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Autores principales: Li, Aiyun, Long, Lin, Liu, Fengshou, Liu, Jianbo, Wu, Xiaochun, Ji, Yinglu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857339/
https://www.ncbi.nlm.nih.gov/pubmed/31807139
http://dx.doi.org/10.1186/s13036-019-0220-1
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author Li, Aiyun
Long, Lin
Liu, Fengshou
Liu, Jianbo
Wu, Xiaochun
Ji, Yinglu
author_facet Li, Aiyun
Long, Lin
Liu, Fengshou
Liu, Jianbo
Wu, Xiaochun
Ji, Yinglu
author_sort Li, Aiyun
collection PubMed
description BACKGROUND: As an emerging research area of artificial enzymes, nanozyme, the catalytic nanomaterials with enzyme-like characteristics, have attracted enormous attention in research. Here, a nanozyme probe has been realized by utilizing antigen-labeled mesoporous silica-encapsulated Au-core Pt-shell (Au@Pt@SiO(2)) nanostructures for the diagnosis of rubella virus (RV). Pt nanoparticles have been suggested to act as potent peroxidase mimetics with high activities. However, smaller Pt nanoparticles are very easily aggregated, which has negative effects on the catalytic activities. RESULTS: In this work, the use of gold nanorod as the support favours the well dispersion of the small Pt nanoparticles to improve the stability of them. Furthermore, the designed the silica shell could also isolate the recognition antigens from the surface reactive sites, retaining catalytic activity of the inner nanozyme. In addition, compared with antigen-labeled horseradish peroxidase (HRP), the antigen-labeled Au@Pt@SiO(2) nanozyme was more stable and robust. A capture enzyme-linked immunosorbent assay (ELISA) for the determination of RV showed that the antigen-labeled Au@Pt@SiO(2) nanozyme-based ELISA exhibited good sensitivity. CONCLUSIONS: The highly sensitive peroxidase-like activity of antigen-labeled Au@Pt@SiO(2) nanozyme, along with their catalytic stability and robustness, can facilitate their utilization in biochemical assays and clinical diagnosis.
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spelling pubmed-68573392019-12-05 Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis Li, Aiyun Long, Lin Liu, Fengshou Liu, Jianbo Wu, Xiaochun Ji, Yinglu J Biol Eng Research BACKGROUND: As an emerging research area of artificial enzymes, nanozyme, the catalytic nanomaterials with enzyme-like characteristics, have attracted enormous attention in research. Here, a nanozyme probe has been realized by utilizing antigen-labeled mesoporous silica-encapsulated Au-core Pt-shell (Au@Pt@SiO(2)) nanostructures for the diagnosis of rubella virus (RV). Pt nanoparticles have been suggested to act as potent peroxidase mimetics with high activities. However, smaller Pt nanoparticles are very easily aggregated, which has negative effects on the catalytic activities. RESULTS: In this work, the use of gold nanorod as the support favours the well dispersion of the small Pt nanoparticles to improve the stability of them. Furthermore, the designed the silica shell could also isolate the recognition antigens from the surface reactive sites, retaining catalytic activity of the inner nanozyme. In addition, compared with antigen-labeled horseradish peroxidase (HRP), the antigen-labeled Au@Pt@SiO(2) nanozyme was more stable and robust. A capture enzyme-linked immunosorbent assay (ELISA) for the determination of RV showed that the antigen-labeled Au@Pt@SiO(2) nanozyme-based ELISA exhibited good sensitivity. CONCLUSIONS: The highly sensitive peroxidase-like activity of antigen-labeled Au@Pt@SiO(2) nanozyme, along with their catalytic stability and robustness, can facilitate their utilization in biochemical assays and clinical diagnosis. BioMed Central 2019-11-14 /pmc/articles/PMC6857339/ /pubmed/31807139 http://dx.doi.org/10.1186/s13036-019-0220-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Aiyun
Long, Lin
Liu, Fengshou
Liu, Jianbo
Wu, Xiaochun
Ji, Yinglu
Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title_full Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title_fullStr Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title_full_unstemmed Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title_short Antigen-labeled mesoporous silica-coated Au-core Pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
title_sort antigen-labeled mesoporous silica-coated au-core pt-shell nanostructure: a novel nanoprobe for highly efficient virus diagnosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857339/
https://www.ncbi.nlm.nih.gov/pubmed/31807139
http://dx.doi.org/10.1186/s13036-019-0220-1
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