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A Rapid Method for Refolding Cell Surface Receptors and Ligands

Production of membrane-associated cell surface receptors and their ligands is often a cumbersome, expensive, and time-consuming process that limits detailed structural and functional characterization of this important class of proteins. Here we report a rapid method for refolding inclusion-body-base...

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Detalles Bibliográficos
Autores principales: Zhai, Lu, Wu, Ling, Li, Feng, Burnham, Robert S., Pizarro, Juan C., Xu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877712/
https://www.ncbi.nlm.nih.gov/pubmed/27215173
http://dx.doi.org/10.1038/srep26482
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author Zhai, Lu
Wu, Ling
Li, Feng
Burnham, Robert S.
Pizarro, Juan C.
Xu, Bin
author_facet Zhai, Lu
Wu, Ling
Li, Feng
Burnham, Robert S.
Pizarro, Juan C.
Xu, Bin
author_sort Zhai, Lu
collection PubMed
description Production of membrane-associated cell surface receptors and their ligands is often a cumbersome, expensive, and time-consuming process that limits detailed structural and functional characterization of this important class of proteins. Here we report a rapid method for refolding inclusion-body-based, recombinant cell surface receptors and ligands in one day, a speed equivalent to that of soluble protein production. This method efficiently couples modular on-column immobilized metal ion affinity purification and solid-phase protein refolding. We demonstrated the general utility of this method for producing multiple functionally active immunoreceptors, ligands, and viral decoys, including challenging cell surface proteins that cannot be produced using typical dialysis- or dilution-based refolding approaches.
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spelling pubmed-48777122016-06-08 A Rapid Method for Refolding Cell Surface Receptors and Ligands Zhai, Lu Wu, Ling Li, Feng Burnham, Robert S. Pizarro, Juan C. Xu, Bin Sci Rep Article Production of membrane-associated cell surface receptors and their ligands is often a cumbersome, expensive, and time-consuming process that limits detailed structural and functional characterization of this important class of proteins. Here we report a rapid method for refolding inclusion-body-based, recombinant cell surface receptors and ligands in one day, a speed equivalent to that of soluble protein production. This method efficiently couples modular on-column immobilized metal ion affinity purification and solid-phase protein refolding. We demonstrated the general utility of this method for producing multiple functionally active immunoreceptors, ligands, and viral decoys, including challenging cell surface proteins that cannot be produced using typical dialysis- or dilution-based refolding approaches. Nature Publishing Group 2016-05-24 /pmc/articles/PMC4877712/ /pubmed/27215173 http://dx.doi.org/10.1038/srep26482 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhai, Lu
Wu, Ling
Li, Feng
Burnham, Robert S.
Pizarro, Juan C.
Xu, Bin
A Rapid Method for Refolding Cell Surface Receptors and Ligands
title A Rapid Method for Refolding Cell Surface Receptors and Ligands
title_full A Rapid Method for Refolding Cell Surface Receptors and Ligands
title_fullStr A Rapid Method for Refolding Cell Surface Receptors and Ligands
title_full_unstemmed A Rapid Method for Refolding Cell Surface Receptors and Ligands
title_short A Rapid Method for Refolding Cell Surface Receptors and Ligands
title_sort rapid method for refolding cell surface receptors and ligands
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877712/
https://www.ncbi.nlm.nih.gov/pubmed/27215173
http://dx.doi.org/10.1038/srep26482
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