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High-yield overproduction and purification of human aquaporins from Pichia pastoris
Aquaporins (AQPs) are membrane-bound water channels that play crucial roles in maintaining the water homeostasis of the human body. Here, we present a protocol for high-yield recombinant expression of human AQPs in the methylotropic yeast Pichia pastoris and subsequent AQP purification. The protocol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026565/ https://www.ncbi.nlm.nih.gov/pubmed/35463467 http://dx.doi.org/10.1016/j.xpro.2022.101298 |
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author | Al-Jubair, Tamim Steffen, Jonas Hyld Missel, Julie Winkel Kitchen, Philip Salman, Mootaz M. Bill, Roslyn M. Gourdon, Pontus Törnroth-Horsefield, Susanna |
author_facet | Al-Jubair, Tamim Steffen, Jonas Hyld Missel, Julie Winkel Kitchen, Philip Salman, Mootaz M. Bill, Roslyn M. Gourdon, Pontus Törnroth-Horsefield, Susanna |
author_sort | Al-Jubair, Tamim |
collection | PubMed |
description | Aquaporins (AQPs) are membrane-bound water channels that play crucial roles in maintaining the water homeostasis of the human body. Here, we present a protocol for high-yield recombinant expression of human AQPs in the methylotropic yeast Pichia pastoris and subsequent AQP purification. The protocol typically yields 1–5 mg AQP per g of yeast cell at >95% purity and is compatible with any membrane protein cloned into Pichia pastoris, although expression levels may vary. For complete details on the use and execution of this protocol, please refer to Kitchen et al. (2020) and Frick et al. (2014). |
format | Online Article Text |
id | pubmed-9026565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90265652022-04-23 High-yield overproduction and purification of human aquaporins from Pichia pastoris Al-Jubair, Tamim Steffen, Jonas Hyld Missel, Julie Winkel Kitchen, Philip Salman, Mootaz M. Bill, Roslyn M. Gourdon, Pontus Törnroth-Horsefield, Susanna STAR Protoc Protocol Aquaporins (AQPs) are membrane-bound water channels that play crucial roles in maintaining the water homeostasis of the human body. Here, we present a protocol for high-yield recombinant expression of human AQPs in the methylotropic yeast Pichia pastoris and subsequent AQP purification. The protocol typically yields 1–5 mg AQP per g of yeast cell at >95% purity and is compatible with any membrane protein cloned into Pichia pastoris, although expression levels may vary. For complete details on the use and execution of this protocol, please refer to Kitchen et al. (2020) and Frick et al. (2014). Elsevier 2022-04-12 /pmc/articles/PMC9026565/ /pubmed/35463467 http://dx.doi.org/10.1016/j.xpro.2022.101298 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Al-Jubair, Tamim Steffen, Jonas Hyld Missel, Julie Winkel Kitchen, Philip Salman, Mootaz M. Bill, Roslyn M. Gourdon, Pontus Törnroth-Horsefield, Susanna High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title | High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title_full | High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title_fullStr | High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title_full_unstemmed | High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title_short | High-yield overproduction and purification of human aquaporins from Pichia pastoris |
title_sort | high-yield overproduction and purification of human aquaporins from pichia pastoris |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026565/ https://www.ncbi.nlm.nih.gov/pubmed/35463467 http://dx.doi.org/10.1016/j.xpro.2022.101298 |
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