The use of UCOE vectors in combination with a preadapted serum free, suspension cell line allows for rapid production of large quantities of protein
Open accessAbstract
UCOE vectors contain non-tissue specific chromatin-opening-elements that permit rapid expression of a protein in anintegration independent manner. Efficient expression can bederived from a single copy of an integrated gene site resulting ina higher percentage of cells expressing the marker gene in theselected pool in comparison to standard non-UCOE containingvectors. This, in combination with the utilization of a serum-free, suspension adapted parent cell line allows for rapidproduction of large quantities of protein in a short period oftime. Utilizing this system more than 300 mg of a recombinantantibody has been produced in less than 1 month from transfectionpools in shake flask. Selected subclones have been scaled intosmall bioreactors in less than 2 months, producing significantquantities of monoclonal antibody using a protocol generic for theparent cell line. The increased efficiency obtained with the UCOEvector reduces the number of transfectants which need to bescreened in order to obtain high productivity subclones.Transfection of a standard host cell line, preadapted to grow in alarge-scale setting, allows for rapid cell line developmentdecreasing the transition time from research into development andmanufacturing. Alternatively, the traditional approach of using aparent cell line which requires serum-free and suspensionadaptation after transfection further increases the need forscreening a large number of subclones, because many of thesubclones will not be able to grow under conditions that allowlarge-scale protein production. The use of a preadapted cell linecan reduce the time required to develop a cell line from months toweeks.
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UCOEs were found to be helpful for increasing the productivity of recombinant protein cell lines.
“UCOEs were also found to be helpful for increasing the productivity of recombinant protein cell lines (Benton et al., 2002;She et al., 2009).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Benton et al., 2002
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Research works printed but not linked: 1
- Gorfien SF, Dzimian JL, Tilkins ML, Godwin GP & Fike R (1998) Recombinant Protein Production by CHO Cells Cultures in a Chemically Defined Medium. In: Kitagawa Y, Matsuda T, Iijima S (eds.) Animal Cell Technology: Basic & Applied Aspects. Kluwer Academic Publishers (Netherlands) pp. 247-252.
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Therapeutic glycoprotein production in mammalian cells
Lalonde, M.-E., & Durocher, Y. (2017) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2017.04.028 · Cited by 296 · see citing works
Fan, L., Frye, C. C., & Racher, A. J. (2013) · Pharmaceutical Bioprocessing · doi:10.4155/pbp.13.56 · Cited by 35 · see citing works
Harraghy, N., Calabrese, D., Fisch, I., Girod, P., LeFourn, V., Regamey, A., & Mermod, N. (2015) · Biotechnology Journal · doi:10.1002/biot.201400649 · Cited by 32 · see citing works
- Authors
- Benton, T., Chen, T., McEntee, M., Fox, B., King, D., Crombie, R., Thomas, T. C., & Bebbington, C.
- Affiliations
- Corixa Corporation (US)
- Keele University (GB)
- Venue
- Cytotechnology
- Published
- 2002-01
- Volume
- 38
- Issue
- 1-3
- Pages
- 43-46
- ISSN
- 0920-9069 (ISSN-L)
- 1573-0778
- PMC
- PMC3449923
- OpenAlex
- W2113446079
- Cited by
- 98
- References
- 0
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 1 · 2019: 3 · 2018: 1 · 2017: 7 · 2016: 2 · 2015: 11 · 2014: 5 · 2013: 10 · 2012: 7
- FWCI
- 0.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cytotechnology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Keywords
- cell line development, shake flask culture, bioreactor scale-up, large-scale protein production
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