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High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae
BACKGROUND: Animal-free recombinant proteins provide a safe and effective alternative to tissue or serum-derived products for both therapeutic and biomanufacturing applications. While recombinant insulin and albumin already exist to replace their human counterparts in cell culture media, until recen...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000842/ https://www.ncbi.nlm.nih.gov/pubmed/21083917 http://dx.doi.org/10.1186/1475-2859-9-87 |
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author | Finnis, Christopher JA Payne, Tom Hay, Joanna Dodsworth, Neil Wilkinson, Diane Morton, Philip Saxton, Malcolm J Tooth, David J Evans, Robert W Goldenberg, Hans Scheiber-Mojdehkar, Barbara Ternes, Nina Sleep, Darrell |
author_facet | Finnis, Christopher JA Payne, Tom Hay, Joanna Dodsworth, Neil Wilkinson, Diane Morton, Philip Saxton, Malcolm J Tooth, David J Evans, Robert W Goldenberg, Hans Scheiber-Mojdehkar, Barbara Ternes, Nina Sleep, Darrell |
author_sort | Finnis, Christopher JA |
collection | PubMed |
description | BACKGROUND: Animal-free recombinant proteins provide a safe and effective alternative to tissue or serum-derived products for both therapeutic and biomanufacturing applications. While recombinant insulin and albumin already exist to replace their human counterparts in cell culture media, until recently there has been no equivalent for serum transferrin. RESULTS: The first microbial system for the high-level secretion of a recombinant transferrin (rTf) has been developed from Saccharomyces cerevisiae strains originally engineered for the commercial production of recombinant human albumin (Novozymes' Recombumin(® )USP-NF) and albumin fusion proteins (Novozymes' albufuse(®)). A full-length non-N-linked glycosylated rTf was secreted at levels around ten-fold higher than from commonly used laboratory strains. Modification of the yeast 2 μm-based expression vector to allow overexpression of the ER chaperone, protein disulphide isomerase, further increased the secretion of rTf approximately twelve-fold in high cell density fermentation. The rTf produced was functionally equivalent to plasma-derived transferrin. CONCLUSIONS: A Saccharomyces cerevisiae expression system has enabled the cGMP manufacture of an animal-free rTf for industrial cell culture application without the risk of prion and viral contamination, and provides a high-quality platform for the development of transferrin-based therapeutics. |
format | Text |
id | pubmed-3000842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30008422010-12-11 High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae Finnis, Christopher JA Payne, Tom Hay, Joanna Dodsworth, Neil Wilkinson, Diane Morton, Philip Saxton, Malcolm J Tooth, David J Evans, Robert W Goldenberg, Hans Scheiber-Mojdehkar, Barbara Ternes, Nina Sleep, Darrell Microb Cell Fact Research BACKGROUND: Animal-free recombinant proteins provide a safe and effective alternative to tissue or serum-derived products for both therapeutic and biomanufacturing applications. While recombinant insulin and albumin already exist to replace their human counterparts in cell culture media, until recently there has been no equivalent for serum transferrin. RESULTS: The first microbial system for the high-level secretion of a recombinant transferrin (rTf) has been developed from Saccharomyces cerevisiae strains originally engineered for the commercial production of recombinant human albumin (Novozymes' Recombumin(® )USP-NF) and albumin fusion proteins (Novozymes' albufuse(®)). A full-length non-N-linked glycosylated rTf was secreted at levels around ten-fold higher than from commonly used laboratory strains. Modification of the yeast 2 μm-based expression vector to allow overexpression of the ER chaperone, protein disulphide isomerase, further increased the secretion of rTf approximately twelve-fold in high cell density fermentation. The rTf produced was functionally equivalent to plasma-derived transferrin. CONCLUSIONS: A Saccharomyces cerevisiae expression system has enabled the cGMP manufacture of an animal-free rTf for industrial cell culture application without the risk of prion and viral contamination, and provides a high-quality platform for the development of transferrin-based therapeutics. BioMed Central 2010-11-17 /pmc/articles/PMC3000842/ /pubmed/21083917 http://dx.doi.org/10.1186/1475-2859-9-87 Text en Copyright ©2010 Finnis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Finnis, Christopher JA Payne, Tom Hay, Joanna Dodsworth, Neil Wilkinson, Diane Morton, Philip Saxton, Malcolm J Tooth, David J Evans, Robert W Goldenberg, Hans Scheiber-Mojdehkar, Barbara Ternes, Nina Sleep, Darrell High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title | High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title_full | High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title_fullStr | High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title_full_unstemmed | High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title_short | High-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
title_sort | high-level production of animal-free recombinant transferrin from saccharomyces cerevisiae |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000842/ https://www.ncbi.nlm.nih.gov/pubmed/21083917 http://dx.doi.org/10.1186/1475-2859-9-87 |
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