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Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line
LPR1 (LOW PHOSPHATE ROOT 1), a bacterial-type plant ferroxidase, is crucial for local root phosphate (Pi) sensing. Here, we present a detailed protocol for native (tag-free) protein purification of LPR1 from leaf extracts by differential ammonium sulfate precipitation, size exclusion, and cation exc...
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/PMC9530668/ https://www.ncbi.nlm.nih.gov/pubmed/36181680 http://dx.doi.org/10.1016/j.xpro.2022.101733 |
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author | Tang, Nancy Naumann, Christin |
author_facet | Tang, Nancy Naumann, Christin |
author_sort | Tang, Nancy |
collection | PubMed |
description | LPR1 (LOW PHOSPHATE ROOT 1), a bacterial-type plant ferroxidase, is crucial for local root phosphate (Pi) sensing. Here, we present a detailed protocol for native (tag-free) protein purification of LPR1 from leaf extracts by differential ammonium sulfate precipitation, size exclusion, and cation exchange chromatography of a transgenic Arabidopsis thaliana line overexpressing LPR1. We outline steps for LPR1 purification tracking via immune blot analysis and ferroxidase activity assay. The protocol yields highly pure and active LPR1 protein for biochemical analysis. For complete details on the use and execution of this protocol, please refer to Naumann et al. (2022). |
format | Online Article Text |
id | pubmed-9530668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95306682022-10-05 Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line Tang, Nancy Naumann, Christin STAR Protoc Protocol LPR1 (LOW PHOSPHATE ROOT 1), a bacterial-type plant ferroxidase, is crucial for local root phosphate (Pi) sensing. Here, we present a detailed protocol for native (tag-free) protein purification of LPR1 from leaf extracts by differential ammonium sulfate precipitation, size exclusion, and cation exchange chromatography of a transgenic Arabidopsis thaliana line overexpressing LPR1. We outline steps for LPR1 purification tracking via immune blot analysis and ferroxidase activity assay. The protocol yields highly pure and active LPR1 protein for biochemical analysis. For complete details on the use and execution of this protocol, please refer to Naumann et al. (2022). Elsevier 2022-09-29 /pmc/articles/PMC9530668/ /pubmed/36181680 http://dx.doi.org/10.1016/j.xpro.2022.101733 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Tang, Nancy Naumann, Christin Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title | Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title_full | Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title_fullStr | Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title_full_unstemmed | Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title_short | Native protein purification of ferroxidase LPR1 from leaf extracts of a transgenic Arabidopsis thaliana line |
title_sort | native protein purification of ferroxidase lpr1 from leaf extracts of a transgenic arabidopsis thaliana line |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530668/ https://www.ncbi.nlm.nih.gov/pubmed/36181680 http://dx.doi.org/10.1016/j.xpro.2022.101733 |
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