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Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics
Cell line development is an essential stage in biopharmaceutical development that often lies on the critical path. Failure to fully characterise the lead clone during initial screening can lead to lengthy project delays during scale-up, which can potentially compromise commercial manufacturing succe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277482/ https://www.ncbi.nlm.nih.gov/pubmed/37342509 http://dx.doi.org/10.3389/fbioe.2023.1160223 |
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author | Goldrick, Stephen Alosert, Haneen Lovelady, Clare Bond, Nicholas J. Senussi, Tarik Hatton, Diane Klein, John Cheeks, Matthew Turner, Richard Savery, James Farid, Suzanne S. |
author_facet | Goldrick, Stephen Alosert, Haneen Lovelady, Clare Bond, Nicholas J. Senussi, Tarik Hatton, Diane Klein, John Cheeks, Matthew Turner, Richard Savery, James Farid, Suzanne S. |
author_sort | Goldrick, Stephen |
collection | PubMed |
description | Cell line development is an essential stage in biopharmaceutical development that often lies on the critical path. Failure to fully characterise the lead clone during initial screening can lead to lengthy project delays during scale-up, which can potentially compromise commercial manufacturing success. In this study, we propose a novel cell line development methodology, referenced as CLD ( 4 ), which involves four steps enabling autonomous data-driven selection of the lead clone. The first step involves the digitalisation of the process and storage of all available information within a structured data lake. The second step calculates a new metric referenced as the cell line manufacturability index (MI ( CL )) quantifying the performance of each clone by considering the selection criteria relevant to productivity, growth and product quality. The third step implements machine learning (ML) to identify any potential risks associated with process operation and relevant critical quality attributes (CQAs). The final step of CLD ( 4 ) takes into account the available metadata and summaries all relevant statistics generated in steps 1–3 in an automated report utilising a natural language generation (NLG) algorithm. The CLD ( 4 ) methodology was implemented to select the lead clone of a recombinant Chinese hamster ovary (CHO) cell line producing high levels of an antibody-peptide fusion with a known product quality issue related to end-point trisulfide bond (TSB) concentration. CLD ( 4 ) identified sub-optimal process conditions leading to increased levels of trisulfide bond that would not be identified through conventional cell line development methodologies. CLD ( 4 ) embodies the core principles of Industry 4.0 and demonstrates the benefits of increased digitalisation, data lake integration, predictive analytics and autonomous report generation to enable more informed decision making. |
format | Online Article Text |
id | pubmed-10277482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102774822023-06-20 Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics Goldrick, Stephen Alosert, Haneen Lovelady, Clare Bond, Nicholas J. Senussi, Tarik Hatton, Diane Klein, John Cheeks, Matthew Turner, Richard Savery, James Farid, Suzanne S. Front Bioeng Biotechnol Bioengineering and Biotechnology Cell line development is an essential stage in biopharmaceutical development that often lies on the critical path. Failure to fully characterise the lead clone during initial screening can lead to lengthy project delays during scale-up, which can potentially compromise commercial manufacturing success. In this study, we propose a novel cell line development methodology, referenced as CLD ( 4 ), which involves four steps enabling autonomous data-driven selection of the lead clone. The first step involves the digitalisation of the process and storage of all available information within a structured data lake. The second step calculates a new metric referenced as the cell line manufacturability index (MI ( CL )) quantifying the performance of each clone by considering the selection criteria relevant to productivity, growth and product quality. The third step implements machine learning (ML) to identify any potential risks associated with process operation and relevant critical quality attributes (CQAs). The final step of CLD ( 4 ) takes into account the available metadata and summaries all relevant statistics generated in steps 1–3 in an automated report utilising a natural language generation (NLG) algorithm. The CLD ( 4 ) methodology was implemented to select the lead clone of a recombinant Chinese hamster ovary (CHO) cell line producing high levels of an antibody-peptide fusion with a known product quality issue related to end-point trisulfide bond (TSB) concentration. CLD ( 4 ) identified sub-optimal process conditions leading to increased levels of trisulfide bond that would not be identified through conventional cell line development methodologies. CLD ( 4 ) embodies the core principles of Industry 4.0 and demonstrates the benefits of increased digitalisation, data lake integration, predictive analytics and autonomous report generation to enable more informed decision making. Frontiers Media S.A. 2023-06-05 /pmc/articles/PMC10277482/ /pubmed/37342509 http://dx.doi.org/10.3389/fbioe.2023.1160223 Text en Copyright © 2023 Goldrick, Alosert, Lovelady, Bond, Senussi, Hatton, Klein, Cheeks, Turner, Savery and Farid. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Goldrick, Stephen Alosert, Haneen Lovelady, Clare Bond, Nicholas J. Senussi, Tarik Hatton, Diane Klein, John Cheeks, Matthew Turner, Richard Savery, James Farid, Suzanne S. Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title | Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title_full | Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title_fullStr | Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title_full_unstemmed | Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title_short | Next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
title_sort | next-generation cell line selection methodology leveraging data lakes, natural language generation and advanced data analytics |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277482/ https://www.ncbi.nlm.nih.gov/pubmed/37342509 http://dx.doi.org/10.3389/fbioe.2023.1160223 |
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