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Nanocellulose aerogels as 3D amyloid templates

Proteins in solution tend to coat solid surfaces upon exposure. Depending on the nature of the surface, the environmental conditions, and the nature of the protein these adsorbed proteins may self-assemble into ordered, fibre-like structures called amyloids. Nanoparticulate surfaces, with their high...

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Autores principales: Sinha, Ashutosh, Kummer, Nico, Wu, Tingting, De France, Kevin J., Pinotsi, Dorothea, Thoma, Janine L., Fischer, Peter, Campioni, Silvia, Nyström, Gustav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653027/
https://www.ncbi.nlm.nih.gov/pubmed/37909800
http://dx.doi.org/10.1039/d3nr02109b
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author Sinha, Ashutosh
Kummer, Nico
Wu, Tingting
De France, Kevin J.
Pinotsi, Dorothea
Thoma, Janine L.
Fischer, Peter
Campioni, Silvia
Nyström, Gustav
author_facet Sinha, Ashutosh
Kummer, Nico
Wu, Tingting
De France, Kevin J.
Pinotsi, Dorothea
Thoma, Janine L.
Fischer, Peter
Campioni, Silvia
Nyström, Gustav
author_sort Sinha, Ashutosh
collection PubMed
description Proteins in solution tend to coat solid surfaces upon exposure. Depending on the nature of the surface, the environmental conditions, and the nature of the protein these adsorbed proteins may self-assemble into ordered, fibre-like structures called amyloids. Nanoparticulate surfaces, with their high surface to volume ratio, are particularly favourable to amyloid formation. Most prior research has focussed on either inorganic or organic nanoparticles in solution. In this research, we instead focus on aerogels created from TEMPO-oxidized cellulose nanofibers (TO-CNF) to serve as bio-based, three-dimensional amyloid templates with a tuneable surface chemistry. Previous research on the use of cellulose as a protein adsorption template has shown no evidence of a change in the secondary protein structure. Herein, however, with the aid of the reducing agent TCEP, we were able to induce the formation of amyloid-like ‘worms’ on the surface of TO-CNF aerogels. Furthermore, we demonstrate that the addition of the TO-CNF aerogel can also induce bulk aggregation under conditions where it previously did not exist. Finally, we show that the addition of the aerogel increases the rate of ‘worm’ formation in conditions where previous research has found a long lag-phase. Therefore, TO-CNF aerogels are shown to be excellent templates for inducing ordered protein aggregation.
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spelling pubmed-106530272023-11-01 Nanocellulose aerogels as 3D amyloid templates Sinha, Ashutosh Kummer, Nico Wu, Tingting De France, Kevin J. Pinotsi, Dorothea Thoma, Janine L. Fischer, Peter Campioni, Silvia Nyström, Gustav Nanoscale Chemistry Proteins in solution tend to coat solid surfaces upon exposure. Depending on the nature of the surface, the environmental conditions, and the nature of the protein these adsorbed proteins may self-assemble into ordered, fibre-like structures called amyloids. Nanoparticulate surfaces, with their high surface to volume ratio, are particularly favourable to amyloid formation. Most prior research has focussed on either inorganic or organic nanoparticles in solution. In this research, we instead focus on aerogels created from TEMPO-oxidized cellulose nanofibers (TO-CNF) to serve as bio-based, three-dimensional amyloid templates with a tuneable surface chemistry. Previous research on the use of cellulose as a protein adsorption template has shown no evidence of a change in the secondary protein structure. Herein, however, with the aid of the reducing agent TCEP, we were able to induce the formation of amyloid-like ‘worms’ on the surface of TO-CNF aerogels. Furthermore, we demonstrate that the addition of the TO-CNF aerogel can also induce bulk aggregation under conditions where it previously did not exist. Finally, we show that the addition of the aerogel increases the rate of ‘worm’ formation in conditions where previous research has found a long lag-phase. Therefore, TO-CNF aerogels are shown to be excellent templates for inducing ordered protein aggregation. The Royal Society of Chemistry 2023-11-01 /pmc/articles/PMC10653027/ /pubmed/37909800 http://dx.doi.org/10.1039/d3nr02109b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Sinha, Ashutosh
Kummer, Nico
Wu, Tingting
De France, Kevin J.
Pinotsi, Dorothea
Thoma, Janine L.
Fischer, Peter
Campioni, Silvia
Nyström, Gustav
Nanocellulose aerogels as 3D amyloid templates
title Nanocellulose aerogels as 3D amyloid templates
title_full Nanocellulose aerogels as 3D amyloid templates
title_fullStr Nanocellulose aerogels as 3D amyloid templates
title_full_unstemmed Nanocellulose aerogels as 3D amyloid templates
title_short Nanocellulose aerogels as 3D amyloid templates
title_sort nanocellulose aerogels as 3d amyloid templates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653027/
https://www.ncbi.nlm.nih.gov/pubmed/37909800
http://dx.doi.org/10.1039/d3nr02109b
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