An ultra scale‐down approach identifies host cell protein differences across a panel of mAb producing CHO cell line variants. Issue 3 (9th December 2015)

• Record Type: Journal Article
• Authors: Hogwood, Catherine E.M.; Ahmad, Shahina S.; Tarrant, Richard D.; Bracewell, Daniel G.; Smales, C. Mark
• Is Part Of: Biotechnology journal. Volume 11:Issue 3(2016)
• Page Start: 415
• Page End: 424
• Publication Date: 2015-12-09
• Subjects: Chinese hamster ovary cells -- Host cell protein -- Mammalian cell culture -- Monoclonal antibody -- Ultra scale‐down; Biotechnology -- Periodicals; 660.605
• DOI: 10.1002/biot.201500010
• Languages: English
• ISSNs: 1860-6768

Abstract

Abstract: During the manufacture of biopharmaceutical products, the final product must lie within strict pre‐set specifications, for example the host cell protein (HCP) content. A number of specific HCPs have been identified in particular products and the interactions between product/HCPs have also been recently investigated; however, a comparison of the HCP dynamics between related cell lines and their response to early downstream processing to aid process development and cell line selection has not been published. We have utilised a proteomic approach coupled with an ultra scale‐down study to determine the HCP profile dynamics, at harvest and during early downstream processing, across a panel of recombinant GS‐CHOK1SV antibody producing cell lines. The results reveal that cell culture viability upon harvest has the greatest impact upon shear sensitivity and HCP concentration. Whilst the general HCP population/profile was broadly similar across the cell lines, the actual amounts of some specific HCPs in the supernatant differed and a number of cell line specific differences in the response to early downstream processing were observed. We anticipate that such knowledge can now be applied to cell line selection and downstream processing development to target reduction/removal of general and specific problematic HCPs before and during downstream processing. Abstract : The authors have utilised a proteomic approach coupled with an ultra scale‐down study to determine the HCP profile dynamics, at harvest and during early downstream processing, across a panel of recombinant GS‐CHOK1SV antibody producing cell lines. Whilst the general HCP population/profile is broadly similar across the cell lines, the actual amounts of some specific HCPs in the supernatant differ, and a number of cell line specific differences in the response to early downstream processing are observed.