Improving expression of recombinant human IGF-1 using IGF-1R knockout CHO cell lines
| Autor: | Holger Laux, Thomas Jostock, Anett Ritter, Joerg Schmidt, Burkhard Wilms, Mara Fornaro, Sandrine Romand |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Gene knockdown Cell growth Chemistry Growth factor medicine.medical_treatment Chinese hamster ovary cell Clone (cell biology) Bioengineering Applied Microbiology and Biotechnology Molecular biology law.invention 03 medical and health sciences 030104 developmental biology Cell culture law medicine Recombinant DNA Receptor Biotechnology |
| Zdroj: | Biotechnology and Bioengineering. 113:1094-1101 |
| ISSN: | 0006-3592 |
| Popis: | Chinese Hamster Ovary (CHO) cells are widely used for the large-scale production of recombinant biopharmaceuticals. However, attempts to express IGF-1 (a mutated human Insulin-like growth factor 1 Ea peptide (hIGF-1Ea mut)) in CHO cells resulted in poor cell growth and low productivity (0.1-0.2 g/L). Human IGF-1 variants negatively impacted CHO cell growth via the IGF-1 receptor (IGF-1R). Therefore knockout (KO) of the IGF-1R gene in two different CHO cell lines as well as knockdown (KD) of IGF-1R in one CHO cell line were performed. These cell line engineering approaches decreased significantly the hIGF-1 mediated cell growth inhibition and increased productivity of both KO CHO cell lines as well as of the KD CHO cell line. A productivity increase of 10-fold at pool level and sevenfold at clone level was achieved, resulting in a titer of 1.3 g/L. This data illustrate that cell line engineering approaches are powerful tools to improve the yields of recombinant proteins which are difficult to produce in CHO cells. |
| Databáze: | OpenAIRE |
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