Peng Xing Yue, Li Paul C H
Department of Chemistry, Simon Fraser University, Burnaby, British Columbia, Canada V5A 1S6.
Anal Chem. 2004 Sep 15;76(18):5273-81. doi: 10.1021/ac049384s.
An ideal microchip for single-cell experiments should be able to allow us to culture cells, to select any desired single cell from a group, to retain the cell for convenient cellular signal detection, and to deliver any buffer or reagent directly to the cell at any time during continual detection and observation. Most importantly, any negative impact on the live cell should be minimized. To accomplish all these functions, we developed a three-dimensional liquid flow control concept and employed special liquid flow fields to manipulate and retain a single yeast cell freely in the chip. A zero-speed point was controlled to retain the cell for three-dimensional cell balancing and cell scanning. A dispersive flow delivered reagents at a high speed to very near the cell and provided them to the cell at a low speed. No force stronger than its gravitational force was exerted on the cell, which could be balanced on different positions on an arc-sloping wall, thus minimizing any negative impact on the cell due to strong liquid flows. Specifically, we demonstrate on-chip single-cell culture, cell wall removal, and reagent delivery. Subsequently, single-cell fluorescence detection was performed, and noise filtering and background correction were applied for data processing.
用于单细胞实验的理想微芯片应能够让我们培养细胞,从一组细胞中挑选出任何所需的单个细胞,保留该细胞以便于进行细胞信号检测,并在连续检测和观察期间的任何时候将任何缓冲液或试剂直接输送到细胞。最重要的是,应将对活细胞的任何负面影响降至最低。为实现所有这些功能,我们开发了一种三维液体流动控制概念,并采用特殊的液体流场在芯片中自由操纵和保留单个酵母细胞。通过控制一个零速点来保留细胞,以进行三维细胞平衡和细胞扫描。分散流以高速将试剂输送到非常靠近细胞的位置,并以低速将试剂提供给细胞。没有对细胞施加比其重力更强的力,细胞可以在弧形倾斜壁上的不同位置实现平衡,从而将强液体流对细胞的任何负面影响降至最低。具体而言,我们展示了芯片上的单细胞培养、细胞壁去除和试剂输送。随后,进行了单细胞荧光检测,并应用噪声过滤和背景校正进行数据处理。