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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...

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Detalles Bibliográficos
Autores principales: Tang, Nancy, Naumann, Christin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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).
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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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