中国仓鼠卵巢细胞
转染
重组DNA
分子生物学
组蛋白脱乙酰酶抑制剂
信使核糖核酸
生物
细胞培养
组蛋白脱乙酰基酶
化学
组蛋白
DNA
生物化学
基因
遗传学
作者
Sarah Wulhfard,Lucia Baldi,David L. Hacker,Florian Μ. Wurm
标识
DOI:10.1016/j.jbiotec.2010.05.003
摘要
Valproic acid (VPA) is a small molecule that inhibits histone deacetylase activity. Here we report that VPA increases recombinant mRNA and protein levels in transiently transfected CHO DG44 cells. In the presence of VPA, transient recombinant antibody yields of up to 40 mg/L were achieved in simple batch cultures. The steady-state levels of the IgG light and heavy chain mRNAs were nearly 10 times higher than in the untreated control transfection even though the level of transfected plasmid DNA was the same in the presence or absence of VPA. The combination of VPA treatment and incubation of the transfected cells in mildly hypothermic conditions resulted in recombinant antibody yields of over 90 mg/L by 6 days post-transfection in batch cultures. The results demonstrated that the treatment of transfected CHO DG44 cells with VPA is a cost-effective strategy for enhancing transient gene expression by increasing the transgene mRNA levels.
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