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Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines
The development of highly productive, genetically stable manufacturing cell lines is on the critical path to IND filing for protein‐based biologic drugs. Here, we describe the Leap‐In Transposase® platform, a novel transposon‐based mammalian (e.g., Chinese hamster ovary) cell line development system...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252637/ https://www.ncbi.nlm.nih.gov/pubmed/33704772 http://dx.doi.org/10.1002/bit.27742 |
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author | Rajendran, Sowmya Balasubramanian, Sowmya Webster, Lynn Lee, Maggie Vavilala, Divya Kulikov, Nicolay Choi, Jessica Tang, Calvin Hunter, Molly Wang, Rebecca Kaur, Harpreet Karunakaran, Surya Sitaraman, Varsha Minshull, Jeremy Boldog, Ferenc |
author_facet | Rajendran, Sowmya Balasubramanian, Sowmya Webster, Lynn Lee, Maggie Vavilala, Divya Kulikov, Nicolay Choi, Jessica Tang, Calvin Hunter, Molly Wang, Rebecca Kaur, Harpreet Karunakaran, Surya Sitaraman, Varsha Minshull, Jeremy Boldog, Ferenc |
author_sort | Rajendran, Sowmya |
collection | PubMed |
description | The development of highly productive, genetically stable manufacturing cell lines is on the critical path to IND filing for protein‐based biologic drugs. Here, we describe the Leap‐In Transposase® platform, a novel transposon‐based mammalian (e.g., Chinese hamster ovary) cell line development system that produces high‐titer stable pools with productivity and product quality attributes that are highly comparable to clones that are subsequently derived therefrom. The productivity distributions of clones are strongly biased toward high producers, and genetic and expression stability is consistently high. By avoiding the poor integration rates, concatemer formation, detrimental transgene recombination, low average expression level, unpredictable product quality, and inconsistent genetic stability characteristic of nonhomologous recombination methods, Leap‐In provides several opportunities to de‐risk programs early and reduce timelines and resources. |
format | Online Article Text |
id | pubmed-8252637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82526372021-07-09 Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines Rajendran, Sowmya Balasubramanian, Sowmya Webster, Lynn Lee, Maggie Vavilala, Divya Kulikov, Nicolay Choi, Jessica Tang, Calvin Hunter, Molly Wang, Rebecca Kaur, Harpreet Karunakaran, Surya Sitaraman, Varsha Minshull, Jeremy Boldog, Ferenc Biotechnol Bioeng ARTICLES The development of highly productive, genetically stable manufacturing cell lines is on the critical path to IND filing for protein‐based biologic drugs. Here, we describe the Leap‐In Transposase® platform, a novel transposon‐based mammalian (e.g., Chinese hamster ovary) cell line development system that produces high‐titer stable pools with productivity and product quality attributes that are highly comparable to clones that are subsequently derived therefrom. The productivity distributions of clones are strongly biased toward high producers, and genetic and expression stability is consistently high. By avoiding the poor integration rates, concatemer formation, detrimental transgene recombination, low average expression level, unpredictable product quality, and inconsistent genetic stability characteristic of nonhomologous recombination methods, Leap‐In provides several opportunities to de‐risk programs early and reduce timelines and resources. John Wiley and Sons Inc. 2021-04-02 2021-06 /pmc/articles/PMC8252637/ /pubmed/33704772 http://dx.doi.org/10.1002/bit.27742 Text en © 2021 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ARTICLES Rajendran, Sowmya Balasubramanian, Sowmya Webster, Lynn Lee, Maggie Vavilala, Divya Kulikov, Nicolay Choi, Jessica Tang, Calvin Hunter, Molly Wang, Rebecca Kaur, Harpreet Karunakaran, Surya Sitaraman, Varsha Minshull, Jeremy Boldog, Ferenc Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title | Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title_full | Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title_fullStr | Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title_full_unstemmed | Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title_short | Accelerating and de‐risking CMC development with transposon‐derived manufacturing cell lines |
title_sort | accelerating and de‐risking cmc development with transposon‐derived manufacturing cell lines |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252637/ https://www.ncbi.nlm.nih.gov/pubmed/33704772 http://dx.doi.org/10.1002/bit.27742 |
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