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Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility
Efficient production of large quantities of therapeutic antibodies is becoming a major goal of the pharmaceutical industry. We developed a proprietary expression system using a polyprotein precursor-based approach to antibody expression in mammalian cells. In this approach, the coding regions for he...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906313/ https://www.ncbi.nlm.nih.gov/pubmed/23774760 http://dx.doi.org/10.4161/mabs.25161 |
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author | Gion, Wendy R. Davis-Taber, Rachel A. Regier, Dean A. Fung, Emma Medina, Limary Santora, Ling C. Bose, Sahana Ivanov, Alexander V. Perilli-Palmer, Barbara A. Chumsae, Chris M. Matuck, Joseph G. Kunes, Yune Z. Carson, Gerald R. |
author_facet | Gion, Wendy R. Davis-Taber, Rachel A. Regier, Dean A. Fung, Emma Medina, Limary Santora, Ling C. Bose, Sahana Ivanov, Alexander V. Perilli-Palmer, Barbara A. Chumsae, Chris M. Matuck, Joseph G. Kunes, Yune Z. Carson, Gerald R. |
author_sort | Gion, Wendy R. |
collection | PubMed |
description | Efficient production of large quantities of therapeutic antibodies is becoming a major goal of the pharmaceutical industry. We developed a proprietary expression system using a polyprotein precursor-based approach to antibody expression in mammalian cells. In this approach, the coding regions for heavy and light chains are included within a single open reading frame (sORF) separated by an in-frame intein gene. A single mRNA and subsequent polypeptide are produced upon transient and stable transfection into HEK293 and CHO cells, respectively. Heavy and light chains are separated by the autocatalytic action of the intein and antibody processing proceeds to produce active, secreted antibody. Here, we report advances in sORF technology toward establishment of a viable manufacturing platform for therapeutic antibodies in CHO cells. Increasing expression levels and improving antibody processing by intein and signal peptide selection are discussed. |
format | Online Article Text |
id | pubmed-3906313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39063132014-02-04 Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility Gion, Wendy R. Davis-Taber, Rachel A. Regier, Dean A. Fung, Emma Medina, Limary Santora, Ling C. Bose, Sahana Ivanov, Alexander V. Perilli-Palmer, Barbara A. Chumsae, Chris M. Matuck, Joseph G. Kunes, Yune Z. Carson, Gerald R. MAbs Report Efficient production of large quantities of therapeutic antibodies is becoming a major goal of the pharmaceutical industry. We developed a proprietary expression system using a polyprotein precursor-based approach to antibody expression in mammalian cells. In this approach, the coding regions for heavy and light chains are included within a single open reading frame (sORF) separated by an in-frame intein gene. A single mRNA and subsequent polypeptide are produced upon transient and stable transfection into HEK293 and CHO cells, respectively. Heavy and light chains are separated by the autocatalytic action of the intein and antibody processing proceeds to produce active, secreted antibody. Here, we report advances in sORF technology toward establishment of a viable manufacturing platform for therapeutic antibodies in CHO cells. Increasing expression levels and improving antibody processing by intein and signal peptide selection are discussed. Landes Bioscience 2013-07-01 2013-05-31 /pmc/articles/PMC3906313/ /pubmed/23774760 http://dx.doi.org/10.4161/mabs.25161 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Report Gion, Wendy R. Davis-Taber, Rachel A. Regier, Dean A. Fung, Emma Medina, Limary Santora, Ling C. Bose, Sahana Ivanov, Alexander V. Perilli-Palmer, Barbara A. Chumsae, Chris M. Matuck, Joseph G. Kunes, Yune Z. Carson, Gerald R. Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title | Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title_full | Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title_fullStr | Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title_full_unstemmed | Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title_short | Expression of antibodies using single open reading frame (sORF) vector design: Demonstration of manufacturing feasibility |
title_sort | expression of antibodies using single open reading frame (sorf) vector design: demonstration of manufacturing feasibility |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906313/ https://www.ncbi.nlm.nih.gov/pubmed/23774760 http://dx.doi.org/10.4161/mabs.25161 |
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