High cell density transient transfection of CHO cells for TGF‐β1 expression
Autor: | Dörte Solle, Lena Stuckenberg, Abdalla A Elshereef, Thomas Scheper, André Jochums, Antonina Lavrentieva |
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Rok vydání: | 2019 |
Předmět: |
0106 biological sciences
animal structures Environmental Engineering viruses Bioengineering 01 natural sciences Green fluorescent protein law.invention 03 medical and health sciences law 010608 biotechnology Centrifugation Viability assay 030304 developmental biology 0303 health sciences Chemistry Chinese hamster ovary cell fungi Biological activity Transfection Molecular biology embryonic structures Recombinant DNA Research Article Biotechnology Transforming growth factor |
Zdroj: | Eng Life Sci |
ISSN: | 1618-2863 1618-0240 |
DOI: | 10.1002/elsc.201800174 |
Popis: | High cell densities for transient transfection with polyethyleneimine (PEI) can be used for rapid and maximal production of recombinant proteins. High cell densities can be obtained by different cultivation systems, such as batch or perfusion systems. Herein, densities up to 18 million cells/mL were obtained by centrifugation for transfection evaluation. PEI transfection efficiency was easily determined by transfected enhanced green fluorescence protein (EGFP) reporter plasmid DNA (pDNA). A linear correlation between fluorescence intensity and transfection efficiency was improved. The transfection efficiency of PEI was highly dependent on the transfection conditions and directly related to the level of recombinant protein. Several factors were required to optimize the transient transfection process; these factors included the media type (which is compatible with low or high cell density transfection), the preculture CHO‐K1 suspension cell density, and the pDNA to PEI level. Based on design of experiment (DoE) analyses, the optimal transfection conditions for 10 × 10(6) cells/mL in the CHOMACS CD medium achieved 73% transfection efficiency and a cell viability of over 80%. These results were confirmed for the production of transforming growth factor‐beta 1 (TGF‐β1) in a shake flask. The purified TGF‐β1 protein concentration from 60 mL supernatant was 27 µg/mL, and the protein was biologically active. |
Databáze: | OpenAIRE |
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