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Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage

Proteins are ubiquitous in molecular biotechnology, biotechnology and as therapeutics, but there are significant challenges in their storage and distribution, with freezing often required. This is traditionally achieved by the addition of cryoprotective agents such as glycerol (or trehalose) or cova...

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Autores principales: Mitchell, Daniel E., Fayter, Alice E. R., Deller, Robert C., Hasan, Muhammad, Gutierrez-Marcos, Jose, Gibson, Matthew I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394881/
https://www.ncbi.nlm.nih.gov/pubmed/30931129
http://dx.doi.org/10.1039/c8mh00727f
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author Mitchell, Daniel E.
Fayter, Alice E. R.
Deller, Robert C.
Hasan, Muhammad
Gutierrez-Marcos, Jose
Gibson, Matthew I.
author_facet Mitchell, Daniel E.
Fayter, Alice E. R.
Deller, Robert C.
Hasan, Muhammad
Gutierrez-Marcos, Jose
Gibson, Matthew I.
author_sort Mitchell, Daniel E.
collection PubMed
description Proteins are ubiquitous in molecular biotechnology, biotechnology and as therapeutics, but there are significant challenges in their storage and distribution, with freezing often required. This is traditionally achieved by the addition of cryoprotective agents such as glycerol (or trehalose) or covalent modification of mutated proteins with cryoprotectants. Here, ice recrystallization inhibiting polymers, inspired by antifreeze proteins, are used synergistically with poly(ethylene glycol) as an alternative to glycerol. The primary mechanism of action appears to be preventing irreversible aggregation due to ice growth. The polymer formulation is successfully used to cryopreserve a range of important proteins including insulin, Taq DNA polymerase and an IgG antibody. The polymers do not require covalent conjugation, nor modification of the protein and are already used in a wide range of biomedical applications, which will facilitate translation to a range of biologics.
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spelling pubmed-63948812019-03-29 Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage Mitchell, Daniel E. Fayter, Alice E. R. Deller, Robert C. Hasan, Muhammad Gutierrez-Marcos, Jose Gibson, Matthew I. Mater Horiz Chemistry Proteins are ubiquitous in molecular biotechnology, biotechnology and as therapeutics, but there are significant challenges in their storage and distribution, with freezing often required. This is traditionally achieved by the addition of cryoprotective agents such as glycerol (or trehalose) or covalent modification of mutated proteins with cryoprotectants. Here, ice recrystallization inhibiting polymers, inspired by antifreeze proteins, are used synergistically with poly(ethylene glycol) as an alternative to glycerol. The primary mechanism of action appears to be preventing irreversible aggregation due to ice growth. The polymer formulation is successfully used to cryopreserve a range of important proteins including insulin, Taq DNA polymerase and an IgG antibody. The polymers do not require covalent conjugation, nor modification of the protein and are already used in a wide range of biomedical applications, which will facilitate translation to a range of biologics. Royal Society of Chemistry 2019-02-01 2018-11-08 /pmc/articles/PMC6394881/ /pubmed/30931129 http://dx.doi.org/10.1039/c8mh00727f Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Mitchell, Daniel E.
Fayter, Alice E. R.
Deller, Robert C.
Hasan, Muhammad
Gutierrez-Marcos, Jose
Gibson, Matthew I.
Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title_full Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title_fullStr Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title_full_unstemmed Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title_short Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
title_sort ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394881/
https://www.ncbi.nlm.nih.gov/pubmed/30931129
http://dx.doi.org/10.1039/c8mh00727f
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