## Abstract An expression vector was specifically designed for use in Chinese hamster ovary (CHO) cells to enhance the level of protein production in a transient expression system. Two key components that can increase protein production transiently are the promoter used to drive recombinant gene ex
Temperature control of growth and productivity in mutant Chinese hamster ovary cells synthesizing a recombinant protein
β Scribed by Nigel Jenkins; Alison Hovey
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 876 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0006-3592
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β¦ Synopsis
The use of a temperature switch to control the growth and productivity of temperature-sensitive (ts) mutants was investigated to extend the productive life span of recombinant Chinese hamster ovary (CHO) cells in batch culture. Bromodeoxyuridine was used at 39Β°C to select mutagenized CHO-K1 cells, which resulted in the isolation of 31 temperature-sensitive mutants that were growth inhibited at 39Β°C. Two of these mutants were successfully transfected with the gene for tissue inhibitor of metalloproteinases (TIMP) using glutamine synthetase amplification, and a permanent recombinant cell line established (5GI-Bl) that maintains the ts phenotype.
Continuous exposure to the nonpermissive temperature (npt) of 39Β°C led to a rapid decline in cell viability. However, a temperature regime using alternating incubations at 34Β°C and 39Β°C arrested the 5G1-B1 cells while retaining a high cell viability for up to 170 h in culture. The specific production rate of the growtharrested cells was 3-4 times that of control cultures maintained at a constant 34Β°C over the crucial 72-130-h period of culture, which resulted in a 35% increase in the maximum product yield. Glucose uptake and lactate production both decreased in arrested cells. Flow cytometric analysis indicated that 5G1-B1 cells arrested in the GI or Go phase of the cell cycle, and no major structural damage was caused to these cells by the alternating temperature regime.
These results demonstrate that growth-arrested ts CHO cells have increased productivity compared t o growing cultures and maintain viability for longer periods. The system offers the prospect of enhancing the productivity of recombinant mammalian cells grown in simple batch fermentors.
π SIMILAR VOLUMES
Overexpression of recombinant proteins in animal cells is commonly achieved by using gene amplification techniques. Gene amplified cells possess up to several thousand genes coding for the target protein. Constitutive expression of these genes leads to high levels of the corresponding mRNA species