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Thermal stability, storage and release of proteins with tailored fit in silica

Biological substances based on proteins, including vaccines, antibodies, and enzymes, typically degrade at room temperature over time due to denaturation, as proteins unfold with loss of secondary and tertiary structure. Their storage and distribution therefore relies on a “cold chain” of continuous...

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Autores principales: Chen, Yun-Chu, Smith, Tristan, Hicks, Robert H., Doekhie, Aswin, Koumanov, Francoise, Wells, Stephen A., Edler, Karen J., van den Elsen, Jean, Holman, Geoffrey D., Marchbank, Kevin J., Sartbaeva, Asel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402271/
https://www.ncbi.nlm.nih.gov/pubmed/28436442
http://dx.doi.org/10.1038/srep46568
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author Chen, Yun-Chu
Smith, Tristan
Hicks, Robert H.
Doekhie, Aswin
Koumanov, Francoise
Wells, Stephen A.
Edler, Karen J.
van den Elsen, Jean
Holman, Geoffrey D.
Marchbank, Kevin J.
Sartbaeva, Asel
author_facet Chen, Yun-Chu
Smith, Tristan
Hicks, Robert H.
Doekhie, Aswin
Koumanov, Francoise
Wells, Stephen A.
Edler, Karen J.
van den Elsen, Jean
Holman, Geoffrey D.
Marchbank, Kevin J.
Sartbaeva, Asel
author_sort Chen, Yun-Chu
collection PubMed
description Biological substances based on proteins, including vaccines, antibodies, and enzymes, typically degrade at room temperature over time due to denaturation, as proteins unfold with loss of secondary and tertiary structure. Their storage and distribution therefore relies on a “cold chain” of continuous refrigeration; this is costly and not always effective, as any break in the chain leads to rapid loss of effectiveness and potency. Efforts have been made to make vaccines thermally stable using treatments including freeze-drying (lyophilisation), biomineralisation, and encapsulation in sugar glass and organic polymers. Here for the first time we show that proteins can be enclosed in a deposited silica “cage”, rendering them stable against denaturing thermal treatment and long-term ambient-temperature storage, and subsequently released into solution with their structure and function intact. This “ensilication” method produces a storable solid protein-loaded material without the need for desiccation or freeze-drying. Ensilication offers the prospect of a solution to the “cold chain” problem for biological materials, in particular for vaccines.
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spelling pubmed-54022712017-04-26 Thermal stability, storage and release of proteins with tailored fit in silica Chen, Yun-Chu Smith, Tristan Hicks, Robert H. Doekhie, Aswin Koumanov, Francoise Wells, Stephen A. Edler, Karen J. van den Elsen, Jean Holman, Geoffrey D. Marchbank, Kevin J. Sartbaeva, Asel Sci Rep Article Biological substances based on proteins, including vaccines, antibodies, and enzymes, typically degrade at room temperature over time due to denaturation, as proteins unfold with loss of secondary and tertiary structure. Their storage and distribution therefore relies on a “cold chain” of continuous refrigeration; this is costly and not always effective, as any break in the chain leads to rapid loss of effectiveness and potency. Efforts have been made to make vaccines thermally stable using treatments including freeze-drying (lyophilisation), biomineralisation, and encapsulation in sugar glass and organic polymers. Here for the first time we show that proteins can be enclosed in a deposited silica “cage”, rendering them stable against denaturing thermal treatment and long-term ambient-temperature storage, and subsequently released into solution with their structure and function intact. This “ensilication” method produces a storable solid protein-loaded material without the need for desiccation or freeze-drying. Ensilication offers the prospect of a solution to the “cold chain” problem for biological materials, in particular for vaccines. Nature Publishing Group 2017-04-24 /pmc/articles/PMC5402271/ /pubmed/28436442 http://dx.doi.org/10.1038/srep46568 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chen, Yun-Chu
Smith, Tristan
Hicks, Robert H.
Doekhie, Aswin
Koumanov, Francoise
Wells, Stephen A.
Edler, Karen J.
van den Elsen, Jean
Holman, Geoffrey D.
Marchbank, Kevin J.
Sartbaeva, Asel
Thermal stability, storage and release of proteins with tailored fit in silica
title Thermal stability, storage and release of proteins with tailored fit in silica
title_full Thermal stability, storage and release of proteins with tailored fit in silica
title_fullStr Thermal stability, storage and release of proteins with tailored fit in silica
title_full_unstemmed Thermal stability, storage and release of proteins with tailored fit in silica
title_short Thermal stability, storage and release of proteins with tailored fit in silica
title_sort thermal stability, storage and release of proteins with tailored fit in silica
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402271/
https://www.ncbi.nlm.nih.gov/pubmed/28436442
http://dx.doi.org/10.1038/srep46568
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