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Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein

In this study, a novel approach for preparation of green fluorescent protein (GFP)-doped silica nanoparticles with a narrow size distribution is presented. GFP was chosen as a model protein due to its autofluorescence. Protein-doped nanoparticles have a high application potential in the field of int...

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Autores principales: Schmidt, Sarah, Tavernaro, Isabella, Cavelius, Christian, Weber, Eva, Kümper, Alexander, Schmitz, Carmen, Fleddermann, Jana, Kraegeloh, Annette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612907/
https://www.ncbi.nlm.nih.gov/pubmed/28948498
http://dx.doi.org/10.1186/s11671-017-2280-9
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author Schmidt, Sarah
Tavernaro, Isabella
Cavelius, Christian
Weber, Eva
Kümper, Alexander
Schmitz, Carmen
Fleddermann, Jana
Kraegeloh, Annette
author_facet Schmidt, Sarah
Tavernaro, Isabella
Cavelius, Christian
Weber, Eva
Kümper, Alexander
Schmitz, Carmen
Fleddermann, Jana
Kraegeloh, Annette
author_sort Schmidt, Sarah
collection PubMed
description In this study, a novel approach for preparation of green fluorescent protein (GFP)-doped silica nanoparticles with a narrow size distribution is presented. GFP was chosen as a model protein due to its autofluorescence. Protein-doped nanoparticles have a high application potential in the field of intracellular protein delivery. In addition, fluorescently labelled particles can be used for bioimaging. The size of these protein-doped nanoparticles was adjusted from 15 to 35 nm using a multistep synthesis process, comprising the particle core synthesis followed by shell regrowth steps. GFP was selectively incorporated into the silica matrix of either the core or the shell or both by a one-pot reaction. The obtained nanoparticles were characterised by determination of particle size, hydrodynamic diameter, ζ-potential, fluorescence and quantum yield. The measurements showed that the fluorescence of GFP was maintained during particle synthesis. Cellular uptake experiments demonstrated that the GFP-doped nanoparticles can be used as stable and effective fluorescent probes. The study reveals the potential of the chosen approach for incorporation of functional biological macromolecules into silica nanoparticles, which opens novel application fields like intracellular protein delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-017-2280-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-56129072017-10-10 Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein Schmidt, Sarah Tavernaro, Isabella Cavelius, Christian Weber, Eva Kümper, Alexander Schmitz, Carmen Fleddermann, Jana Kraegeloh, Annette Nanoscale Res Lett Nano Express In this study, a novel approach for preparation of green fluorescent protein (GFP)-doped silica nanoparticles with a narrow size distribution is presented. GFP was chosen as a model protein due to its autofluorescence. Protein-doped nanoparticles have a high application potential in the field of intracellular protein delivery. In addition, fluorescently labelled particles can be used for bioimaging. The size of these protein-doped nanoparticles was adjusted from 15 to 35 nm using a multistep synthesis process, comprising the particle core synthesis followed by shell regrowth steps. GFP was selectively incorporated into the silica matrix of either the core or the shell or both by a one-pot reaction. The obtained nanoparticles were characterised by determination of particle size, hydrodynamic diameter, ζ-potential, fluorescence and quantum yield. The measurements showed that the fluorescence of GFP was maintained during particle synthesis. Cellular uptake experiments demonstrated that the GFP-doped nanoparticles can be used as stable and effective fluorescent probes. The study reveals the potential of the chosen approach for incorporation of functional biological macromolecules into silica nanoparticles, which opens novel application fields like intracellular protein delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-017-2280-9) contains supplementary material, which is available to authorized users. Springer US 2017-09-25 /pmc/articles/PMC5612907/ /pubmed/28948498 http://dx.doi.org/10.1186/s11671-017-2280-9 Text en © The Author(s). 2017 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.
spellingShingle Nano Express
Schmidt, Sarah
Tavernaro, Isabella
Cavelius, Christian
Weber, Eva
Kümper, Alexander
Schmitz, Carmen
Fleddermann, Jana
Kraegeloh, Annette
Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title_full Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title_fullStr Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title_full_unstemmed Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title_short Silica Nanoparticles for Intracellular Protein Delivery: a Novel Synthesis Approach Using Green Fluorescent Protein
title_sort silica nanoparticles for intracellular protein delivery: a novel synthesis approach using green fluorescent protein
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612907/
https://www.ncbi.nlm.nih.gov/pubmed/28948498
http://dx.doi.org/10.1186/s11671-017-2280-9
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