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An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody

BACKGROUND: Protein Corona (PC) of nanoparticles is a structure which composed of one or more layers of proteins adsorbed on the surface of nanomaterials, and the formation of PC is a universal process of spontaneous randomness. We take advantage of the formation principle of the PC, developed a sim...

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Detalles Bibliográficos
Autores principales: Zhao, Penghua, Huang, Xiaoyan, Li, Yaping, Huo, Xueping, Feng, Qing, Zhao, Xiangrong, Xu, Cuixiang, Wang, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008981/
https://www.ncbi.nlm.nih.gov/pubmed/36923872
http://dx.doi.org/10.1016/j.heliyon.2023.e13860
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author Zhao, Penghua
Huang, Xiaoyan
Li, Yaping
Huo, Xueping
Feng, Qing
Zhao, Xiangrong
Xu, Cuixiang
Wang, Jianhua
author_facet Zhao, Penghua
Huang, Xiaoyan
Li, Yaping
Huo, Xueping
Feng, Qing
Zhao, Xiangrong
Xu, Cuixiang
Wang, Jianhua
author_sort Zhao, Penghua
collection PubMed
description BACKGROUND: Protein Corona (PC) of nanoparticles is a structure which composed of one or more layers of proteins adsorbed on the surface of nanomaterials, and the formation of PC is a universal process of spontaneous randomness. We take advantage of the formation principle of the PC, developed a simple and efficient method for label protein to nanoparticles. METHODS: The artificialed protein corona (APC) on the surface of nanoparticles was synthesized via the artificialed methods of desolvation aggregation and crosslinking with control. RESULTS: The dosage of precipitator and the ratio of protein to magnetic nanoparticles (MNPs)(particle size: 3 nm) were optimized, and the core-shell nanoparticles with narrow particle size (particle size: 10 nm) distribution were obtained. The MNPs with APC were characterized by transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). Additionally, a hemolysis test on prepared MNPs was conducted with APC. The presence of APC coating on the surface of MNPs showed an improving effect to reduce the cytotoxicity. Cellular toxicity of MNPs with APC was also investigated on HFF1 cell lines. And the cells survival in the presence of APC coated MNPs and display neither reduced metabolism nor cytostatic effect. The functional test of the MNPs with APC showed that proteins can be modified and labeled onto magnetic nanoparticles and retain their original activity. CONCLUSIONS: This marking method is gentle and effective. And the properties of the APC propose MNPs as a promising candidate for multifunctional biomedical applications.
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spelling pubmed-100089812023-03-14 An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody Zhao, Penghua Huang, Xiaoyan Li, Yaping Huo, Xueping Feng, Qing Zhao, Xiangrong Xu, Cuixiang Wang, Jianhua Heliyon Research Article BACKGROUND: Protein Corona (PC) of nanoparticles is a structure which composed of one or more layers of proteins adsorbed on the surface of nanomaterials, and the formation of PC is a universal process of spontaneous randomness. We take advantage of the formation principle of the PC, developed a simple and efficient method for label protein to nanoparticles. METHODS: The artificialed protein corona (APC) on the surface of nanoparticles was synthesized via the artificialed methods of desolvation aggregation and crosslinking with control. RESULTS: The dosage of precipitator and the ratio of protein to magnetic nanoparticles (MNPs)(particle size: 3 nm) were optimized, and the core-shell nanoparticles with narrow particle size (particle size: 10 nm) distribution were obtained. The MNPs with APC were characterized by transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). Additionally, a hemolysis test on prepared MNPs was conducted with APC. The presence of APC coating on the surface of MNPs showed an improving effect to reduce the cytotoxicity. Cellular toxicity of MNPs with APC was also investigated on HFF1 cell lines. And the cells survival in the presence of APC coated MNPs and display neither reduced metabolism nor cytostatic effect. The functional test of the MNPs with APC showed that proteins can be modified and labeled onto magnetic nanoparticles and retain their original activity. CONCLUSIONS: This marking method is gentle and effective. And the properties of the APC propose MNPs as a promising candidate for multifunctional biomedical applications. Elsevier 2023-03-01 /pmc/articles/PMC10008981/ /pubmed/36923872 http://dx.doi.org/10.1016/j.heliyon.2023.e13860 Text en © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Zhao, Penghua
Huang, Xiaoyan
Li, Yaping
Huo, Xueping
Feng, Qing
Zhao, Xiangrong
Xu, Cuixiang
Wang, Jianhua
An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title_full An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title_fullStr An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title_full_unstemmed An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title_short An artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
title_sort artificialed protein corona coating the surface of magnetic nanoparicles:a simple and efficient method for label antibody
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008981/
https://www.ncbi.nlm.nih.gov/pubmed/36923872
http://dx.doi.org/10.1016/j.heliyon.2023.e13860
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