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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A microfluidic flow-through device for high throughput electrical lysis of bacterial cells based on continuous dc voltage
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A microfluidic flow-through device for high throughput electrical lysis of bacterial cells based on continuous dc voltage

机译:基于连续直流电压用于细菌细胞高通量电裂解的微流过装置

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摘要

Interest in electrical lysis of biological cells on a microfludic platform has increased because it allows for the rapid recovery of intracellular contents without introducing lytic agents. In this study we demonstrated a simple microfluidic flow-through device which lysed Escherichia coli cells under a continuous dc voltage. The E. coli cells had previously been modified to express green fluorescent protein (GFP). In our design, the cell lysis only happened in a defined section of a microfluidic channel due to the local field amplification by geometric modification. The geometric modification also effectively decreased the required voltage for lysis by several folds. We found that local field strength of 1000-1500 V/cm was required for nearly 100% cell death. This threshold field strength was considerably lower than the value reported in the literature, possibly due to the longer duration of the field [Lee, S.W., Tai, Y.C., 1999. Sens. Actuators A: Phys. 73, 74-79]. Cell lysis was detected by both plate count and fluorescence spectroscopy. The cell membrane was completely disintegrated in the lysis section of the microfluidic device, when the field strength was higher than 2000 V/cm. The devices were fabricated using low-cost soft lithography with channel widths considerably larger than the cell size to avoid clogging and ensure stable performance. Our tool will be ideal for high throughput processing of bacterial cells for chemical analysis of intracellular contents such as DNA and proteins. The application of continuous dc voltage greatly simplified the instrumentation compared to devices using electrical pulses for similar purposes. In principle, the same approach can also be applied for lysis of mammalian cells and electroporative transfection. (c) 2006 Elsevier B.V. All rights reserved.
机译:在微流体平台上对生物细胞进行电裂解的兴趣已经增加,因为它允许在不引入裂解剂的情况下快速恢复细胞内内容物。在这项研究中,我们展示了一种简单的微流穿设备,可在连续的直流电压下裂解大肠杆菌细胞。大肠杆菌细胞先前已被修饰以表达绿色荧光蛋白(GFP)。在我们的设计中,由于通过几何修饰的局部场放大,细胞裂解仅发生在微流体通道的定义区域中。几何修饰还有效地将裂解所需的电压降低了几倍。我们发现,近100%的细胞死亡需要1000-1500 V / cm的局部场强。该阈值场强大大低于文献报道的值,这可能是由于场的持续时间更长[Lee,S.W.,Tai,Y.C.,1999。 73,74-79]。通过平板计数和荧光光谱检测细胞裂解。当场强高于2000 V / cm时,细胞膜在微流控装置的裂解区完全崩解。器件使用低成本的软光刻技术制造,其沟道宽度比单元尺寸大得多,以避免堵塞并确保稳定的性能。我们的工具非常适合用于细菌细胞的高通量处理,以进行细胞内内容物(例如DNA和蛋白质)的化学分析。与出于类似目的使用电脉冲的设备相比,连续直流电压的应用大大简化了仪器。原则上,同样的方法也可以应用于哺乳动物细胞的裂解和电穿孔转染。 (c)2006 Elsevier B.V.保留所有权利。

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