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Nature as blueprint: Global phenotype engineering of CHO production cells based on a multi-omics comparison with plasma cells.
Raab, Nadja; Zeh, Nikolas; Kretz, Robin; Weiß, Linus; Stadermann, Anna; Lindner, Benjamin; Fischer, Simon; Stoll, Dieter; Otte, Kerstin.
Afiliação
  • Raab N; Biberach University of Applied Sciences, Germany. Electronic address: nadja-raab@web.de.
  • Zeh N; Biberach University of Applied Sciences, Germany; Cell Line Development, Bioprocess Development Biologicals, Boehringer Ingelheim Pharma GmbH & Co.KG, Biberach, Germany.
  • Kretz R; Hochschule Albstadt Sigmaringen, Germany; NMI, Natural and Medical Sciences Institute at the University of Tuebingen, Reutlingen, Germany.
  • Weiß L; Biberach University of Applied Sciences, Germany.
  • Stadermann A; Cell Line Development, Bioprocess Development Biologicals, Boehringer Ingelheim Pharma GmbH & Co.KG, Biberach, Germany.
  • Lindner B; Cell Line Development, Bioprocess Development Biologicals, Boehringer Ingelheim Pharma GmbH & Co.KG, Biberach, Germany.
  • Fischer S; Cell Line Development, Bioprocess Development Biologicals, Boehringer Ingelheim Pharma GmbH & Co.KG, Biberach, Germany.
  • Stoll D; NMI, Natural and Medical Sciences Institute at the University of Tuebingen, Reutlingen, Germany.
  • Otte K; Biberach University of Applied Sciences, Germany.
Metab Eng ; 83: 110-122, 2024 May.
Article em En | MEDLINE | ID: mdl-38561148
ABSTRACT
Especially for the production of artificial, difficult to express molecules a further development of the CHO production cell line is required to keep pace with the continuously increasing demands. However, the identification of novel targets for cell line engineering to improve CHO cells is a time and cost intensive process. Since plasma cells are evolutionary optimized for a high antibody expression in mammals, we performed a comprehensive multi-omics comparison between CHO and plasma cells to exploit optimized cellular production traits. Comparing the transcriptome, proteome, miRNome, surfaceome and secretome of both cell lines identified key differences including 392 potential overexpression targets for CHO cell engineering categorized in 15 functional classes like transcription factors, protein processing or secretory pathway. In addition, 3 protein classes including 209 potential knock-down/out targets for CHO engineering were determined likely to affect aggregation or proteolysis. For production phenotype engineering, several of these novel targets were successfully applied to transient and transposase mediated overexpression or knock-down strategies to efficiently improve productivity of CHO cells. Thus, substantial improvement of CHO productivity was achieved by taking nature as a blueprint for cell line engineering.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cricetulus Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cricetulus Idioma: En Ano de publicação: 2024 Tipo de documento: Article