Comparative study of polyethylenimines for transient gene expression in mammalian HEK293 and CHO cells

转染 中国仓鼠卵巢细胞 内化 重组DNA 琼脂糖凝胶电泳 化学 HEK 293细胞 分子生物学 细胞毒性 琼脂糖 生物物理学 凝胶电泳 DNA 色谱法 基因 细胞培养 生物 生物化学 体外 细胞 遗传学
作者
Laurence Delafosse,Ping Xu,Yves Durocher
出处
期刊:Journal of Biotechnology [Elsevier]
卷期号:227: 103-111 被引量:50
标识
DOI:10.1016/j.jbiotec.2016.04.028
摘要

Three commercially available linear polyethylenimines (25 kDa LPEI, 40 kDa PEI“Max” and PEIpro™) were compared regarding their potency to transfect serum-free growing and suspension-adapted HEK293 and CHO cells. We determined the optimal DNA:PEI ratios for maximal expression of the reporter gene SEAP while monitoring cytotoxicity following transfection. PEIs acylation was determined by 1H NMR and their apparent size and polydispersity assessed by size-exclusion chromatography. The propensity of PEIs to condense plasmid DNA was evaluated by agarose-gel electrophoresis. The zeta potentials and particle sizes at optimal DNA:PEI ratio were analyzed. Polyplex attachment to the cells and internalization kinetics were monitored. The quantity of PEIpro™ needed to efficiently transfect the cells was significantly lower than with LPEI and PEI“Max” and, interestingly, the maximal amount of internalized PEIpro™-based polyplexes was approximately half of that observed with its counterparts. PEIpro™ was the largest and least polydisperse polymer, but also the most cytotoxic. The optimal transfection conditions were subsequently used to express three monoclonal antibodies at larger-scale. The use of the deacylated PEI“Max” and PEIpro™ resulted in a significant increase of recombinant protein expression compared to LPEI. These findings demonstrate the importance of properly choosing the most suitable polymers to obtain optimal recombinant protein transient expression.
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