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Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody

Oligosaccharides are generally considered to be un-utilized for growth of mammalian cells because their permeability across the cell membrane is low. However, in our previous study, we discovered that CHO and HEK293 cells consume maltose in culture media without serum and glucose. This is interestin...

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Autores principales: Leong, Dawn Sow Zong, Teo, Brian Kah Hui, Tan, Janice Gek Ling, Kamari, Hayati, Yang, Yuan Sheng, Zhang, Peiqing, Ng, Say Kong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840386/
https://www.ncbi.nlm.nih.gov/pubmed/29511312
http://dx.doi.org/10.1038/s41598-018-22490-8
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author Leong, Dawn Sow Zong
Teo, Brian Kah Hui
Tan, Janice Gek Ling
Kamari, Hayati
Yang, Yuan Sheng
Zhang, Peiqing
Ng, Say Kong
author_facet Leong, Dawn Sow Zong
Teo, Brian Kah Hui
Tan, Janice Gek Ling
Kamari, Hayati
Yang, Yuan Sheng
Zhang, Peiqing
Ng, Say Kong
author_sort Leong, Dawn Sow Zong
collection PubMed
description Oligosaccharides are generally considered to be un-utilized for growth of mammalian cells because their permeability across the cell membrane is low. However, in our previous study, we discovered that CHO and HEK293 cells consume maltose in culture media without serum and glucose. This is interesting because the transporter for maltose in mammalian cells has not been discovered to-date, and the only animal disaccharide transporter that is recently discovered is a sucrose transporter. The application of oligosaccharides in mammalian cell-based biopharmaceutical manufacturing can be beneficial, because it can theoretically increase carbohydrate content of the culture medium and decrease lactate production. Here, we first determined that specific maltose consumption rate in CHO cells was similar to galactose and fructose at 0.257 ng/cell/day. We then demonstrated that CHO cells can be cultivated with reasonable cell growth using higher maltose concentrations. After which, we evaluated the use of maltose supplementation in the production of a recombinant monoclonal antibody in batch and fed-batch cultures, demonstrating improvements in recombinant monoclonal antibody titer of 15% and 23% respectively. Finally, glycosylation profiles of the antibodies were analyzed.
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spelling pubmed-58403862018-03-13 Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody Leong, Dawn Sow Zong Teo, Brian Kah Hui Tan, Janice Gek Ling Kamari, Hayati Yang, Yuan Sheng Zhang, Peiqing Ng, Say Kong Sci Rep Article Oligosaccharides are generally considered to be un-utilized for growth of mammalian cells because their permeability across the cell membrane is low. However, in our previous study, we discovered that CHO and HEK293 cells consume maltose in culture media without serum and glucose. This is interesting because the transporter for maltose in mammalian cells has not been discovered to-date, and the only animal disaccharide transporter that is recently discovered is a sucrose transporter. The application of oligosaccharides in mammalian cell-based biopharmaceutical manufacturing can be beneficial, because it can theoretically increase carbohydrate content of the culture medium and decrease lactate production. Here, we first determined that specific maltose consumption rate in CHO cells was similar to galactose and fructose at 0.257 ng/cell/day. We then demonstrated that CHO cells can be cultivated with reasonable cell growth using higher maltose concentrations. After which, we evaluated the use of maltose supplementation in the production of a recombinant monoclonal antibody in batch and fed-batch cultures, demonstrating improvements in recombinant monoclonal antibody titer of 15% and 23% respectively. Finally, glycosylation profiles of the antibodies were analyzed. Nature Publishing Group UK 2018-03-06 /pmc/articles/PMC5840386/ /pubmed/29511312 http://dx.doi.org/10.1038/s41598-018-22490-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Leong, Dawn Sow Zong
Teo, Brian Kah Hui
Tan, Janice Gek Ling
Kamari, Hayati
Yang, Yuan Sheng
Zhang, Peiqing
Ng, Say Kong
Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title_full Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title_fullStr Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title_full_unstemmed Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title_short Application of maltose as energy source in protein-free CHO-K1 culture to improve the production of recombinant monoclonal antibody
title_sort application of maltose as energy source in protein-free cho-k1 culture to improve the production of recombinant monoclonal antibody
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840386/
https://www.ncbi.nlm.nih.gov/pubmed/29511312
http://dx.doi.org/10.1038/s41598-018-22490-8
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