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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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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. |
format | Online Article Text |
id | pubmed-5402271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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