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Effects of Circular DNA Length on Transfection Efficiency by Electroporation into HeLa Cells

机译:环状DNA长度对电穿孔进入HeLa细胞的转染效率的影响

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摘要

The ability to produce extremely small and circular supercoiled vectors has opened new territory for improving non-viral gene therapy vectors. In this work, we compared transfection of supercoiled DNA vectors ranging from 383 to 4,548 bp, each encoding shRNA against GFP under control of the H1 promoter. We assessed knockdown of GFP by electroporation into HeLa cells. All of our vectors entered cells in comparable numbers when electroporated with equal moles of DNA. Despite similar cell entry, we found length-dependent differences in how efficiently the vectors knocked down GFP. As vector length increased up to 1,869 bp, GFP knockdown efficiency per mole of transfected DNA increased. From 1,869 to 4,257 bp, GFP knockdown efficiency per mole was steady, then decreased with increasing vector length. In comparing GFP knockdown with equal masses of vectors, we found that the shorter vectors transfect more efficiently per nanogram of DNA transfected. Our results rule out cell entry and DNA mass as determining factors for gene knockdown efficiency via electroporation. The length-dependent effects we have uncovered are likely explained by differences in nuclear translocation or transcription. These data add an important step towards clinical applications of non-viral vector delivery.
机译:生产极小且圆形的超螺旋载体的能力为改善非病毒基因治疗载体开辟了新领域。在这项工作中,我们比较了从383到4,548 bp的超螺旋DNA载体的转染,每个载体在H1启动子的控制下编码针对GFP的shRNA。我们通过电穿孔进入HeLa细胞评估了GFP的敲低。当用等摩尔的DNA电穿孔时,我们所有的载体都以相当数量进入细胞。尽管有相似的细胞进入,我们发现载体敲除GFP的效率与长度有关。随着载体长度增加至1869 bp,每摩尔转染DNA的GFP敲低效率增加。从每摩尔GFP的敲低效率从1869 bp到4,257 bp,然后随着载体长度的增加而降低。通过比较GFP敲除与等质量的载体,我们发现较短的载体每转染一纳克的DNA可以更有效地进行转染。我们的结果排除了细胞进入和DNA质量作为通过电穿孔降低基因敲除效率的决定因素。我们发现的长度依赖性效应可能是由于核易位或转录差异引起的。这些数据为非病毒载体的临床应用迈出了重要的一步。

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