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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
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.
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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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