Bioprocessing of Recombinant CHO‐K1, CHO‐DG44, and CHO‐S: CHO Expression Hosts Favor Either mAb Production or Biomass Synthesis. Issue 3 (11th June 2018)
- Record Type:
- Journal Article
- Title:
- Bioprocessing of Recombinant CHO‐K1, CHO‐DG44, and CHO‐S: CHO Expression Hosts Favor Either mAb Production or Biomass Synthesis. Issue 3 (11th June 2018)
- Main Title:
- Bioprocessing of Recombinant CHO‐K1, CHO‐DG44, and CHO‐S: CHO Expression Hosts Favor Either mAb Production or Biomass Synthesis
- Authors:
- Reinhart, David
Damjanovic, Lukas
Kaisermayer, Christian
Sommeregger, Wolfgang
Gili, Andreas
Gasselhuber, Bernhard
Castan, Andreas
Mayrhofer, Patrick
Grünwald‐Gruber, Clemens
Kunert, Renate - Abstract:
- Abstract : Chinese hamster ovary (CHO) cells comprise a variety of lineages including CHO‐DXB11, CHO‐K1, CHO‐DG44, and CHO‐S. Despite all CHO cell lines sharing a common ancestor, extensive mutagenesis, and clonal selection has resulted in substantial genetic heterogeneity among them. Data from sequencing show that different genes are missing in individual CHO cell lines and each cell line harbors a unique set of mutations with relevance to the bioprocess. However, not much literature is available about the influence of genetic differences of CHO on the performance of bioprocess operations. In this study, the host cell‐specific differences among three widely used CHO cell lines (CHO‐K1, CHO‐S, and CHO‐DG44) and recombinantly expressed the same monoclonal antibody (mAb) in an isogenic format by using bacterial artificial chromosomes (BACs) as transfer vector in all cell lines is examined. Cell‐specific growth and product formation are studied in batch, fed‐batch, and semi‐continuous perfusion cultures. Further, two different cell culture media are used to investigate their effects. The authors find CHO cell line‐specific preferences for mAb production or biomass synthesis that are determined by the host cell line. Additionally, quality attributes of the expressed mAb are influenced by the host cell line and media. Abstract : Chinese hamster ovary (CHO) cells comprise a variety of lineages. Despite all CHO cell lines sharing a common ancestor, extensive mutagenesis, and clonalAbstract : Chinese hamster ovary (CHO) cells comprise a variety of lineages including CHO‐DXB11, CHO‐K1, CHO‐DG44, and CHO‐S. Despite all CHO cell lines sharing a common ancestor, extensive mutagenesis, and clonal selection has resulted in substantial genetic heterogeneity among them. Data from sequencing show that different genes are missing in individual CHO cell lines and each cell line harbors a unique set of mutations with relevance to the bioprocess. However, not much literature is available about the influence of genetic differences of CHO on the performance of bioprocess operations. In this study, the host cell‐specific differences among three widely used CHO cell lines (CHO‐K1, CHO‐S, and CHO‐DG44) and recombinantly expressed the same monoclonal antibody (mAb) in an isogenic format by using bacterial artificial chromosomes (BACs) as transfer vector in all cell lines is examined. Cell‐specific growth and product formation are studied in batch, fed‐batch, and semi‐continuous perfusion cultures. Further, two different cell culture media are used to investigate their effects. The authors find CHO cell line‐specific preferences for mAb production or biomass synthesis that are determined by the host cell line. Additionally, quality attributes of the expressed mAb are influenced by the host cell line and media. Abstract : Chinese hamster ovary (CHO) cells comprise a variety of lineages. Despite all CHO cell lines sharing a common ancestor, extensive mutagenesis, and clonal selection has resulted in substantial genetic heterogeneity among them. Data from sequencing show that different genes are missing in individual CHO cell lines and each cell line harbors a unique set of mutations with relevance to the bioprocess. The host cell‐specific differences among three widely used CHO cell lines and recombinantly expressed the same monoclonal antibody (mAb) in an isogenic format by using bacterial artificial chromosomes (BACs) as transfer vector in all cell lines is examined. … (more)
- Is Part Of:
- Biotechnology journal. Volume 14:Issue 3(2019)
- Journal:
- Biotechnology journal
- Issue:
- Volume 14:Issue 3(2019)
- Issue Display:
- Volume 14, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 14
- Issue:
- 3
- Issue Sort Value:
- 2019-0014-0003-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-06-11
- Subjects:
- batch -- bioprocess development -- Chinese hamster ovary -- fed‐batch -- monoclonal antibody -- perfusion -- product quality
Biotechnology -- Periodicals
660.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7314 ↗
http://www.biotechnology-journal.com ↗
http://www3.interscience.wiley.com/cgi-bin/jabout/110544531/2446%5Finfo.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/biot.201700686 ↗
- Languages:
- English
- ISSNs:
- 1860-6768
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.862350
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9589.xml