A CHO cell line engineered to express XBP1 and ERO1-Lα has increased levels of transient protein expression

Katharine Cain, Shirley Peters, Hanna Hailu, Bernie Sweeney, Paul Stephens, James Heads, Kaushik Sarkar, Andy Ventom, Catherine Page, Alan Dickson

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Transient gene expression (TGE) systems currently provide rapid and scalable (up to 100 L) methods for generating multigram quantities of recombinant heterologous proteins. Product titers of up to 1 g/L have been demonstrated in HEK293 cells but reported yields from Chinese hamster ovary (CHO) cells are lower at ∼300 mg/L. We report on the establishment of an engineered CHOS cell line, which has been developed for TGE. This cell line has been engineered to express both X-box binding protein (XBP-1S) and endoplasmic reticulum oxidoreductase (ERO1-Lα) and has been named CHOS-XE. CHOS-XE cells produced increased antibody (MAb) yields (5.3-6.2 fold) in comparison to CHOS cells. Product quality was unchanged as assessed by size, charge, propensity to aggregate, major glycosylation species, and thermal stability. To further develop and test this TGE system, five commercial media were assessed, and one was shown to offer the greatest increase in antibody yields. With the addition of a commercial feed, MAb titers reached 875 mg/L. © 2013 American Institute of Chemical Engineers.
    Original languageEnglish
    Pages (from-to)697-706
    Number of pages9
    JournalBiotechnology progress
    Volume29
    Issue number3
    DOIs
    Publication statusPublished - May 2013

    Keywords

    • Chinese hamster ovary (CHO) cells
    • Endoplasmic reticulum oxidoreductase (ERO1-L alpha)
    • X-box binding protein (XBP-1)

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