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微流控芯片中的液滴电穿孔用于高效细胞转化,无论是否去除细胞壁。

Droplet electroporation in microfluidics for efficient cell transformation with or without cell wall removal.

机构信息

Department of Fine Chemicals Engineering and Chemistry, Chungnam National University, Daejeon, 305-764, Korea.

出版信息

Lab Chip. 2012 Nov 7;12(21):4483-8. doi: 10.1039/c2lc40360a.

Abstract

An efficient cell transformation method is presented that utilizes droplet electroporation on a microfluidic chip. Two types of green microalgae, a wall-less mutant and a wild type of Chlamydomonas reinhardtii, are used as model cells. The PDMS-glass electroporation chip is simply composed of a flow-focusing microstructure for generating cell-encapsulating droplets and a serpentine channel for better mixing of the content in the droplet, and five pairs of parallel microelectrodes on the glass slide, without involving any expensive electrical equipment. The transformation efficiency via the microfluidic electroporation is shown to be more than three orders of magnitude higher for the wall-less mutant, and more than two orders of magnitude higher for the wild type, which has its cell wall intact, than bulk phase electroporation under identical conditions. Furthermore, the microfluidic transformation is remarkably efficient even at a low DNA/cell ratio, facilitating ways of controlling the transgenic copy number, which is important for the stability of the transgene expression.

摘要

提出了一种利用微流控芯片上的液滴电穿孔进行高效细胞转化的方法。以两种绿色微藻,一种无壁突变体和一种野生型莱茵衣藻(Chlamydomonas reinhardtii)作为模型细胞。PDMS-玻璃电穿孔芯片由用于产生细胞包封液滴的流聚焦微结构和用于更好地混合液滴内容物的蛇形通道组成,以及玻璃载玻片上的五对平行微电极,不涉及任何昂贵的电气设备。与相同条件下的体相电穿孔相比,无壁突变体的微流控电穿孔转化效率高出三个数量级以上,而具有完整细胞壁的野生型高出两个数量级以上。此外,即使在低 DNA/细胞比下,微流控转化也非常高效,有利于控制转基因拷贝数,这对于转基因表达的稳定性很重要。

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