Cargando…

Cell function profiling to assess clone stability

In cell line development the identification of stable Chinese hamster ovary cells for production is a critical but onerous task. The stability trial focus upon high‐level attributes can mask profound underlying cellular changes, leading to unstable clones mistakenly being chosen for production. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Dobson, Paul D., Coss, Karen P., Doherty, Carolanne, Clifford, Jerry, Thompson, Ben, James, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383652/
https://www.ncbi.nlm.nih.gov/pubmed/32181887
http://dx.doi.org/10.1002/bit.27336
_version_ 1783563464350892032
author Dobson, Paul D.
Coss, Karen P.
Doherty, Carolanne
Clifford, Jerry
Thompson, Ben
James, David C.
author_facet Dobson, Paul D.
Coss, Karen P.
Doherty, Carolanne
Clifford, Jerry
Thompson, Ben
James, David C.
author_sort Dobson, Paul D.
collection PubMed
description In cell line development the identification of stable Chinese hamster ovary cells for production is a critical but onerous task. The stability trial focus upon high‐level attributes can mask profound underlying cellular changes, leading to unstable clones mistakenly being chosen for production. The challenge is to assay underlying cell pathways and subsystems without pushing up cell line development costs. ChemStress® cell function profiling is a simple, multiwell plate‐based assay that uses a panel of active chemicals to mimic known bioprocess stresses and challenge key pathways. After 3 days of static culture on the plate, functional responses are assayed, for example, titer and growth. Here this approach is used to monitor 131 clones as they change over real stability trials. A novel stability metric is defined over the data to identify stable clones that remain unperturbed across many components of cell function. This allows stability trials to look beneath the titer to identify clones that are internally more stable.
format Online
Article
Text
id pubmed-7383652
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-73836522020-07-27 Cell function profiling to assess clone stability Dobson, Paul D. Coss, Karen P. Doherty, Carolanne Clifford, Jerry Thompson, Ben James, David C. Biotechnol Bioeng COMMUNICATION TO THE EDITOR In cell line development the identification of stable Chinese hamster ovary cells for production is a critical but onerous task. The stability trial focus upon high‐level attributes can mask profound underlying cellular changes, leading to unstable clones mistakenly being chosen for production. The challenge is to assay underlying cell pathways and subsystems without pushing up cell line development costs. ChemStress® cell function profiling is a simple, multiwell plate‐based assay that uses a panel of active chemicals to mimic known bioprocess stresses and challenge key pathways. After 3 days of static culture on the plate, functional responses are assayed, for example, titer and growth. Here this approach is used to monitor 131 clones as they change over real stability trials. A novel stability metric is defined over the data to identify stable clones that remain unperturbed across many components of cell function. This allows stability trials to look beneath the titer to identify clones that are internally more stable. John Wiley and Sons Inc. 2020-04-10 2020-07 /pmc/articles/PMC7383652/ /pubmed/32181887 http://dx.doi.org/10.1002/bit.27336 Text en © 2020 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://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 COMMUNICATION TO THE EDITOR
Dobson, Paul D.
Coss, Karen P.
Doherty, Carolanne
Clifford, Jerry
Thompson, Ben
James, David C.
Cell function profiling to assess clone stability
title Cell function profiling to assess clone stability
title_full Cell function profiling to assess clone stability
title_fullStr Cell function profiling to assess clone stability
title_full_unstemmed Cell function profiling to assess clone stability
title_short Cell function profiling to assess clone stability
title_sort cell function profiling to assess clone stability
topic COMMUNICATION TO THE EDITOR
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383652/
https://www.ncbi.nlm.nih.gov/pubmed/32181887
http://dx.doi.org/10.1002/bit.27336
work_keys_str_mv AT dobsonpauld cellfunctionprofilingtoassessclonestability
AT cosskarenp cellfunctionprofilingtoassessclonestability
AT dohertycarolanne cellfunctionprofilingtoassessclonestability
AT cliffordjerry cellfunctionprofilingtoassessclonestability
AT thompsonben cellfunctionprofilingtoassessclonestability
AT jamesdavidc cellfunctionprofilingtoassessclonestability