Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5521986 | Journal of Immunological Methods | 2017 | 6 Pages |
Abstract
To establish a simple and widely accessible technique for rapidly selecting high producing Chinese hamster ovary (CHO) cells engineered to express a monoclonal antibody (mAb), we have exploited the transient display of recombinant protein on their cell surface. In combination with magnetic bead-based methods, we demonstrate the ability to select for cells of high productivity in the absence of any metabolic-based selection method. This technique is sufficient to obtain genetically stable engineered CHO cells via a single step of cell subcloning and yields sought-after stable, high IgG producing clonal cell lines. This technique may also be applied to other types of cells as well as polyclonal Ab cell pools.
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Authors
Y Poitevin, G Pontini, N Fischer, M Kosco-Vilbois, G Elson,