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Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles

[Image: see text] Magnetic separation is a promising alternative to conventional methods in downstream processing. This can facilitate easier handling, fewer processing steps, and more sustainable processes. Target materials can be extracted directly from crude cell lysates in a single step by magne...

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Autores principales: Schwaminger, Sebastian P., Fraga-García, Paula, Blank-Shim, Silvia A., Straub, Tamara, Haslbeck, Martin, Muraca, Francesco, Dawson, Kenneth A., Berensmeier, Sonja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648446/
https://www.ncbi.nlm.nih.gov/pubmed/31459591
http://dx.doi.org/10.1021/acsomega.8b03348
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author Schwaminger, Sebastian P.
Fraga-García, Paula
Blank-Shim, Silvia A.
Straub, Tamara
Haslbeck, Martin
Muraca, Francesco
Dawson, Kenneth A.
Berensmeier, Sonja
author_facet Schwaminger, Sebastian P.
Fraga-García, Paula
Blank-Shim, Silvia A.
Straub, Tamara
Haslbeck, Martin
Muraca, Francesco
Dawson, Kenneth A.
Berensmeier, Sonja
author_sort Schwaminger, Sebastian P.
collection PubMed
description [Image: see text] Magnetic separation is a promising alternative to conventional methods in downstream processing. This can facilitate easier handling, fewer processing steps, and more sustainable processes. Target materials can be extracted directly from crude cell lysates in a single step by magnetic nanoadsorbents with high-gradient magnetic fishing (HGMF). Additionally, the use of hazardous consumables for reducing downstream processing steps can be avoided. Here, we present proof of principle of one-step magnetic fishing from crude Escherichia coli cell lysate of a green fluorescent protein (GFP) with an attached hexahistidine (His(6))-tag, which is used as the model target molecule. The focus of this investigation is the upscale to a liter scale magnetic fishing process in which a purity of 91% GFP can be achieved in a single purification step from cleared cell lysate. The binding through the His(6)-tag can be demonstrated, since no significant binding of nontagged GFP toward bare iron oxide nanoparticles (BIONs) can be observed. Nonfunctionalized BIONs with primary particle diameters of around 12 nm, as used in the process, can be produced with a simple and low-cost coprecipitation synthesis. Thus, HGMF with BIONs might pave the way for a new and greener era of downstream processing.
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spelling pubmed-66484462019-08-27 Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles Schwaminger, Sebastian P. Fraga-García, Paula Blank-Shim, Silvia A. Straub, Tamara Haslbeck, Martin Muraca, Francesco Dawson, Kenneth A. Berensmeier, Sonja ACS Omega [Image: see text] Magnetic separation is a promising alternative to conventional methods in downstream processing. This can facilitate easier handling, fewer processing steps, and more sustainable processes. Target materials can be extracted directly from crude cell lysates in a single step by magnetic nanoadsorbents with high-gradient magnetic fishing (HGMF). Additionally, the use of hazardous consumables for reducing downstream processing steps can be avoided. Here, we present proof of principle of one-step magnetic fishing from crude Escherichia coli cell lysate of a green fluorescent protein (GFP) with an attached hexahistidine (His(6))-tag, which is used as the model target molecule. The focus of this investigation is the upscale to a liter scale magnetic fishing process in which a purity of 91% GFP can be achieved in a single purification step from cleared cell lysate. The binding through the His(6)-tag can be demonstrated, since no significant binding of nontagged GFP toward bare iron oxide nanoparticles (BIONs) can be observed. Nonfunctionalized BIONs with primary particle diameters of around 12 nm, as used in the process, can be produced with a simple and low-cost coprecipitation synthesis. Thus, HGMF with BIONs might pave the way for a new and greener era of downstream processing. American Chemical Society 2019-02-21 /pmc/articles/PMC6648446/ /pubmed/31459591 http://dx.doi.org/10.1021/acsomega.8b03348 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Schwaminger, Sebastian P.
Fraga-García, Paula
Blank-Shim, Silvia A.
Straub, Tamara
Haslbeck, Martin
Muraca, Francesco
Dawson, Kenneth A.
Berensmeier, Sonja
Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title_full Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title_fullStr Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title_full_unstemmed Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title_short Magnetic One-Step Purification of His-Tagged Protein by Bare Iron Oxide Nanoparticles
title_sort magnetic one-step purification of his-tagged protein by bare iron oxide nanoparticles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648446/
https://www.ncbi.nlm.nih.gov/pubmed/31459591
http://dx.doi.org/10.1021/acsomega.8b03348
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