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Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase
The Brassica rapa hairy root based expression platform, a turnip hairy root based expression system, is able to produce human complex glycoproteins such as the alpha—L—iduronidase (IDUA) with an activity similar to the one produced by Chinese Hamster Ovary (CHO) cells. In this article, a particular...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335068/ https://www.ncbi.nlm.nih.gov/pubmed/30058762 http://dx.doi.org/10.1111/pbi.12994 |
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author | Cardon, Florian Pallisse, Roser Bardor, Muriel Caron, Aurore Vanier, Jessica Ele Ekouna, Jean Pierre Lerouge, Patrice Boitel‐Conti, Michèle Guillet, Marina |
author_facet | Cardon, Florian Pallisse, Roser Bardor, Muriel Caron, Aurore Vanier, Jessica Ele Ekouna, Jean Pierre Lerouge, Patrice Boitel‐Conti, Michèle Guillet, Marina |
author_sort | Cardon, Florian |
collection | PubMed |
description | The Brassica rapa hairy root based expression platform, a turnip hairy root based expression system, is able to produce human complex glycoproteins such as the alpha—L—iduronidase (IDUA) with an activity similar to the one produced by Chinese Hamster Ovary (CHO) cells. In this article, a particular attention has been paid to the N‐ and O‐glycosylation that characterize the alpha‐L‐iduronidase produced using this hairy root based system. This analysis showed that the recombinant protein is characterized by highly homogeneous post translational profiles enabling a strong batch to batch reproducibility. Indeed, on each of the 6 N‐glycosylation sites of the IDUA, a single N‐glycan composed of a core Man(3)GlcNAc(2) carrying one beta(1,2)‐xylose and one alpha(1,3)‐fucose epitope (M3XFGN2) was identified, highlighting the high homogeneity of the production system. Hydroxylation of proline residues and arabinosylation were identified during O‐glycosylation analysis, still with a remarkable reproducibility. This platform is thus positioned as an effective and consistent expression system for the production of human complex therapeutic proteins. |
format | Online Article Text |
id | pubmed-6335068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63350682019-01-23 Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase Cardon, Florian Pallisse, Roser Bardor, Muriel Caron, Aurore Vanier, Jessica Ele Ekouna, Jean Pierre Lerouge, Patrice Boitel‐Conti, Michèle Guillet, Marina Plant Biotechnol J Research Articles The Brassica rapa hairy root based expression platform, a turnip hairy root based expression system, is able to produce human complex glycoproteins such as the alpha—L—iduronidase (IDUA) with an activity similar to the one produced by Chinese Hamster Ovary (CHO) cells. In this article, a particular attention has been paid to the N‐ and O‐glycosylation that characterize the alpha‐L‐iduronidase produced using this hairy root based system. This analysis showed that the recombinant protein is characterized by highly homogeneous post translational profiles enabling a strong batch to batch reproducibility. Indeed, on each of the 6 N‐glycosylation sites of the IDUA, a single N‐glycan composed of a core Man(3)GlcNAc(2) carrying one beta(1,2)‐xylose and one alpha(1,3)‐fucose epitope (M3XFGN2) was identified, highlighting the high homogeneity of the production system. Hydroxylation of proline residues and arabinosylation were identified during O‐glycosylation analysis, still with a remarkable reproducibility. This platform is thus positioned as an effective and consistent expression system for the production of human complex therapeutic proteins. John Wiley and Sons Inc. 2018-08-30 2019-02 /pmc/articles/PMC6335068/ /pubmed/30058762 http://dx.doi.org/10.1111/pbi.12994 Text en © 2018 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Cardon, Florian Pallisse, Roser Bardor, Muriel Caron, Aurore Vanier, Jessica Ele Ekouna, Jean Pierre Lerouge, Patrice Boitel‐Conti, Michèle Guillet, Marina Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title |
Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title_full |
Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title_fullStr |
Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title_full_unstemmed |
Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title_short |
Brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐L‐iduronidase |
title_sort | brassica rapa hairy root based expression system leads to the production of highly homogenous and reproducible profiles of recombinant human alpha‐l‐iduronidase |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335068/ https://www.ncbi.nlm.nih.gov/pubmed/30058762 http://dx.doi.org/10.1111/pbi.12994 |
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