发起人
中国仓鼠卵巢细胞
转基因
基因表达
基因
抄写(语言学)
生物
质粒
转录因子
合成生物学
细胞生物学
分子生物学
化学
计算生物学
生物化学
遗传学
细胞培养
哲学
语言学
作者
Si Nga Sou,Claire Harris,Rebecca E. Williams,Dorota Kozub,Fabio Zurlo,Yash D. Patel,Praveen Kallamvalli Illam Sankaran,Olalekan Daramola,Adam Brown,David C. James,Diane Hatton,Sarah Dunn,Suzanne J. Gibson
摘要
When expressing complex biotherapeutic proteins, traditional expression plasmids and methods may not always yield sufficient levels of high-quality product. High-strength viral promoters commonly used for recombinant protein (rProtein) production in mammalian cells allow for maximal expression, but provide limited scope to alter their transcription dynamics. However, synthetic promoters designed to provide tunable transcriptional activity offer a plasmid engineering approach to more precisely regulate product quality, yield or to reduce product related contaminants. We substituted the viral promoter CMV with synthetic promoters that offer different transcriptional activities to express our gene of interest in Chinese hamster ovary (CHO) cells. Stable pools were established and the benefits of regulating transgene transcription on the quality of biotherapeutics were examined in stable pool fed-batch overgrow experiments. Specific control of gene expression of the heavy chain (HC):light chain (LC) of a Fab, and the ratio between the two HCs in a Duet mAb reduced levels of aberrant protein contaminants; and the controlled expression of the helper gene XBP-1s improved expression of a difficult-to-express mAb. This synthetic promoter technology benefits applications that require custom activity. Our work highlights the advantages of employing synthetic promoters for production of more complex rProteins.
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