DOI | Resolve DOI: https://doi.org/10.1016/j.jbiotec.2017.06.009 |
---|
Author | Search for: Poulain, A.1; Search for: Perret, S.1; Search for: Malenfant, F.1; Search for: Mullick, A.1; Search for: Massie, B.1; Search for: Durocher, Y.1 |
---|
Affiliation | - National Research Council of Canada. Human Health Therapeutics
|
---|
Format | Text, Article |
---|
Subject | CHO; cell pools; inducible expression system; methionine sulfoximine; polyethylenimine; recombinant proteins |
---|
Abstract | To rapidly produce large amounts of recombinant proteins, the generation of stable Chinese Hamster Ovary (CHO) cell pools represents a useful alternative to large-scale transient gene expression (TGE). We have developed a cell line (CHOBRI/rcTA) allowing the inducible expression of recombinant proteins, based on the cumate gene switch. After the identification of optimal plasmid DNA topology (supercoiled vs linearized plasmid) for PEIpro™ mediated transfection and of optimal conditions for methionine sulfoximine (MSX) selection, we were able to generate CHOBRI/rcTA pools producing high levels of recombinant proteins. Volumetric productivities of up to 900mg/L were reproducibly achieved for a Fc fusion protein and up to 350mg/L for an antibody after 14days post-induction in non-optimized fed-batch cultures. In addition, we show that CHO pool volumetric productivities are not affected by a freeze-thaw cycle or following maintenance in culture for over one month in the presence of MSX. Finally, we demonstrate that volumetric protein production with the CR5 cumate-inducible promoter is three- to four-fold higher than with the human CMV or hybrid EF1α-HTLV constitutive promoters. These results suggest that the cumate-inducible CHOBRI/rcTA stable pool platform is a powerful and robust system for the rapid production of gram amounts of recombinant proteins. |
---|
Publication date | 2017-06-15 |
---|
Publisher | Elsevier |
---|
In | |
---|
Language | English |
---|
Peer reviewed | Yes |
---|
NPARC number | 23002175 |
---|
Export citation | Export as RIS |
---|
Report a correction | Report a correction (opens in a new tab) |
---|
Record identifier | ac970221-3075-4921-9c1d-fb59b097f911 |
---|
Record created | 2017-08-29 |
---|
Record modified | 2020-03-16 |
---|