Cell culture process metabolomics together with multivariate data analysis tools opens new routes for bioprocess development and glycosylation prediction.


Journal

Biotechnology progress
ISSN: 1520-6033
Titre abrégé: Biotechnol Prog
Pays: United States
ID NLM: 8506292

Informations de publication

Date de publication:
09 2020
Historique:
received: 01 12 2019
revised: 24 03 2020
accepted: 10 04 2020
pubmed: 5 5 2020
medline: 29 9 2021
entrez: 5 5 2020
Statut: ppublish

Résumé

Multivariate latent variable methods have become a popular and versatile toolset to analyze bioprocess data in industry and academia. This work spans such applications from the evaluation of the role of the standard process variables and metabolites to the metabolomics level, that is, to the extensive number metabolic compounds detectable in the extracellular and intracellular domains. Given the substantial effort currently required for the measurement of the latter groups, a tailored methodology is presented that is capable of providing valuable process insights as well as predicting the glycosylation profile based on only four experiments measured over 12 cell culture days. An important result of the work is the possibility to accurately predict many of the glycan variables based on the information of three experiments. An additional finding is that such predictive models can be generated from the more accessible process and extracellular information only, that is, without including the more experimentally cumbersome intracellular data. With regards to the incorporation of omics data in the standard process analytics framework in the future, this works provides a comprehensive data analysis pathway which can efficiently support numerous bioprocessing tasks.

Identifiants

pubmed: 32364635
doi: 10.1002/btpr.3012
doi:

Substances chimiques

Recombinant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3012

Informations de copyright

© 2020 American Institute of Chemical Engineers.

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Auteurs

Philipp Zürcher (P)

Department of Chemistry and Applied Biosciences, Institute of Chemical and Bioengineering, ETH Zürich, Switzerland.

Michael Sokolov (M)

Department of Chemistry and Applied Biosciences, Institute of Chemical and Bioengineering, ETH Zürich, Switzerland.
DataHow AG, Zurich, Switzerland.

David Brühlmann (D)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Raphael Ducommun (R)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Matthieu Stettler (M)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Jonathan Souquet (J)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Martin Jordan (M)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Hervé Broly (H)

Merck Biopharma, Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.

Massimo Morbidelli (M)

Department of Chemistry and Applied Biosciences, Institute of Chemical and Bioengineering, ETH Zürich, Switzerland.
DataHow AG, Zurich, Switzerland.

Alessandro Butté (A)

Department of Chemistry and Applied Biosciences, Institute of Chemical and Bioengineering, ETH Zürich, Switzerland.
DataHow AG, Zurich, Switzerland.

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