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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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