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Falling water ice affinity purification of ice-binding proteins
Ice-binding proteins (IBPs) permit their hosts to thrive in the presence of ice. The ability of IBPs to control ice growth makes them potential additives in industries ranging from food storage and cryopreservation to anti-icing systems. For IBPs to be used in commercial applications, however, metho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056459/ https://www.ncbi.nlm.nih.gov/pubmed/30038212 http://dx.doi.org/10.1038/s41598-018-29312-x |
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author | Adar, Chen Sirotinskaya, Vera Bar Dolev, Maya Friehmann, Tomer Braslavsky, Ido |
author_facet | Adar, Chen Sirotinskaya, Vera Bar Dolev, Maya Friehmann, Tomer Braslavsky, Ido |
author_sort | Adar, Chen |
collection | PubMed |
description | Ice-binding proteins (IBPs) permit their hosts to thrive in the presence of ice. The ability of IBPs to control ice growth makes them potential additives in industries ranging from food storage and cryopreservation to anti-icing systems. For IBPs to be used in commercial applications, however, methods are needed to produce sufficient quantities of high-quality proteins. Here, we describe a new method for IBP purification, termed falling water ice affinity purification (FWIP). The method is based on the affinity of IBPs for ice and does not require molecular tags. A crude IBP solution is allowed to flow over a chilled vertical surface of a commercial ice machine. The temperature of the surface is lowered gradually until ice crystals are produced, to which the IBPs bind but other solutes do not. We found that a maximum of 35 mg of IBP was incorporated in 1 kg of ice. Two rounds of FWIP resulted in >95% purity. An ice machine that produces 60 kg of ice per day can be used to purify one gram of IBP per day. In combination with efficient concentration of the protein solution by tangential flow filtration the FWIP method is suitable for the purification of grams of IBPs for research purposes and applications. |
format | Online Article Text |
id | pubmed-6056459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60564592018-07-30 Falling water ice affinity purification of ice-binding proteins Adar, Chen Sirotinskaya, Vera Bar Dolev, Maya Friehmann, Tomer Braslavsky, Ido Sci Rep Article Ice-binding proteins (IBPs) permit their hosts to thrive in the presence of ice. The ability of IBPs to control ice growth makes them potential additives in industries ranging from food storage and cryopreservation to anti-icing systems. For IBPs to be used in commercial applications, however, methods are needed to produce sufficient quantities of high-quality proteins. Here, we describe a new method for IBP purification, termed falling water ice affinity purification (FWIP). The method is based on the affinity of IBPs for ice and does not require molecular tags. A crude IBP solution is allowed to flow over a chilled vertical surface of a commercial ice machine. The temperature of the surface is lowered gradually until ice crystals are produced, to which the IBPs bind but other solutes do not. We found that a maximum of 35 mg of IBP was incorporated in 1 kg of ice. Two rounds of FWIP resulted in >95% purity. An ice machine that produces 60 kg of ice per day can be used to purify one gram of IBP per day. In combination with efficient concentration of the protein solution by tangential flow filtration the FWIP method is suitable for the purification of grams of IBPs for research purposes and applications. Nature Publishing Group UK 2018-07-23 /pmc/articles/PMC6056459/ /pubmed/30038212 http://dx.doi.org/10.1038/s41598-018-29312-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Adar, Chen Sirotinskaya, Vera Bar Dolev, Maya Friehmann, Tomer Braslavsky, Ido Falling water ice affinity purification of ice-binding proteins |
title | Falling water ice affinity purification of ice-binding proteins |
title_full | Falling water ice affinity purification of ice-binding proteins |
title_fullStr | Falling water ice affinity purification of ice-binding proteins |
title_full_unstemmed | Falling water ice affinity purification of ice-binding proteins |
title_short | Falling water ice affinity purification of ice-binding proteins |
title_sort | falling water ice affinity purification of ice-binding proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056459/ https://www.ncbi.nlm.nih.gov/pubmed/30038212 http://dx.doi.org/10.1038/s41598-018-29312-x |
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