Transfection of cells using flow-through electroporation based on constant voltage

被引:61
作者
Geng, Tao [2 ]
Zhan, Yihong [2 ]
Wang, Jun [2 ]
Lu, Chang [1 ]
机构
[1] Virginia Tech, Dept Chem Engn, Blacksburg, VA 24061 USA
[2] Purdue Univ, Birck Nanotechnol Ctr, W Lafayette, IN 47907 USA
基金
美国农业部; 美国国家科学基金会;
关键词
VIRUS VECTOR INTEGRATION; GENE-TRANSFER; STEM-CELLS; MICROFLUIDIC ELECTROPORATION; MAMMALIAN-CELLS; CYSTIC-FIBROSIS; DNA DELIVERY; IN-VIVO; THERAPY; SCID-X1;
D O I
10.1038/nprot.2011.360
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electroporation is a high-efficiency and low-toxicity physical gene transfer method. Classical electroporation protocols are limited by the small volume of cell samples processed (less than 107 cells per reaction) and low DNA uptake due to partial permeabilization of the cell membrane. Here we describe a flow-through electroporation protocol for continuous transfection of cells, using disposable devices, a syringe pump and a low-cost power supply that provides a constant voltage. We show transfection of cell samples with rates ranging from 40 mu l min(-1) to 20 ml min(-1) with high efficiency. By inducing complex migrations of cells during the flow, we also show permeabilization of the entire cell membrane and markedly increased DNA uptake. The fabrication of the devices takes 1 d and the flow-through electroporation typically takes 1-2 h.
引用
收藏
页码:1192 / 1208
页数:17
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