Poly(Beta-Amino Ester)s as High-Yield Transfection Reagents for Recombinant Protein Production

转染 中国仓鼠卵巢细胞 HEK 293细胞 重组DNA 分子生物学 基因传递 报告基因 细胞培养 绿色荧光蛋白 生物 化学 生物化学 基因 基因表达 受体 遗传学
作者
Kathryn M. Luly,Yang Hui-lin,Stephen J. Lee,Wentao Wang,Seth D. Ludwig,Haley E. Tarbox,David R. Wilson,Jordan J. Green,Jamie B. Spangler
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 17: 4469-4479 被引量:7
标识
DOI:10.2147/ijn.s377371
摘要

Transient transfection is an essential tool for recombinant protein production, as it allows rapid screening for expression without stable integration of genetic material into a target cell genome. Poly(ethylenimine) (PEI) is the current gold standard for transient gene transfer, but transfection efficiency and the resulting protein yield are limited by the polymer's toxicity. This study investigated the use of a class of cationic polymers, poly(beta-amino ester)s (PBAEs), as reagents for transient transfection in comparison to linear 25 kDa PEI, a commonly used transfection reagent.Transfection efficiency and protein production were assessed in human embryonic kidney 293F (HEK) and Chinese hamster ovary-S (CHO) cell suspensions using PBAE-based nanoparticles in comparison to linear 25 kDa PEI. Production of both a cytosolic reporter and secreted antibodies was investigated.In both HEK and CHO cells, several PBAEs demonstrated superior transfection efficiency and enhanced production of a cytosolic reporter compared to linear 25 kDa PEI. This result extended to secreted proteins, as a model PBAE increased the production of 3 different secreted antibodies compared to linear 25 kDa PEI at culture scales ranging from 20 to 2000 mL. In particular, non-viral gene transfer using the lead PBAE/plasmid DNA nanoparticle formulation led to robust transfection of mammalian cells across different constructs, doses, volumes, and cell types.These results show that PBAEs enhance transfection efficiency and increase protein yield compared to a widespread commercially available reagent, making them attractive candidates as reagents for use in recombinant protein production.
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