Optimized rapid production of recombinant secreted proteins in CHO cells grown in suspension: The case of RBD

被引:1
|
作者
Rosini, Elena [1 ]
Pollegioni, Loredano [1 ]
机构
[1] Univ Insubria, Dept Biotechnol & Life Sci, Via JH Dunant 3, I-21100 Varese, Italy
关键词
cell transfection; polyethyleneimine; RBD glycoprotein; recombinant protein production; secreted soluble proteins; TRANSIENT GENE-EXPRESSION; GLYCOPROTEIN PRODUCTION; MAMMALIAN-CELLS; LARGE-SCALE; TRANSFECTION; PLASMID; CULTURE; BINDING; LEVEL; SPIKE;
D O I
10.1002/bab.2409
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chinese Hamster Ovary cells (CHO) have become the most common workhorse for the commercial production of therapeutic proteins, as well as for the production of recombinant proteins for biomedical research. The ability to grow at high density in suspension, the adaptability to serum free media, and the ease transfection and scale up, made CHO cell line highly productive and robust for large-scale production. Here, we present an optimized workflow used to successfully express and purify a number of human proteins with a yield up to 5 mg/L of culture. The entire protocol, from the synthetic gene design to the assessment of purified protein quality, can be completed in 2 weeks. The established cell culture platform has been efficiently adapted to rapidly produce the receptor-binding domain (RBD) in SARS-CoV-2 S protein, a protein required by many laboratories in 2020 to better understand the initial step of infection related to COVID-19 pandemic. An overall yield of 2 mg of high quality soluble RBD per liter of culture was obtained, a production 10-times cheaper than commercial preparations, this representing an intriguing strategy for future challenges.
引用
收藏
页码:909 / 918
页数:10
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