Center for Biosignatures Discovery Automation, Arizona State University, PO Box 876501. Tempe, AZ, USA.
Lab Chip. 2011 Jul 7;11(13):2276-81. doi: 10.1039/c1lc20207c. Epub 2011 May 23.
Real-time PCR at the single bacterial cell level is an indispensable tool to quantitatively reveal the heterogeneity of isogenetic cells. Conventional PCR platforms that utilize microtiter plates or PCR tubes have been widely used, but their large reaction volumes are not suited for sensitive single-cell analysis. Microfluidic devices provide high density, low volume PCR chambers, but they are usually expensive and require dedicated equipment to manipulate liquid and perform detection. To address these limitations, we developed an inexpensive chip-level device that is compatible with a commercial real-time PCR thermal cycler to perform quantitative PCR for single bacterial cells. The chip contains twelve surface-adhering droplets, defined by hydrophilic patterning, that serve as real-time PCR reaction chambers when they are immersed in oil. A one-step process that premixed reagents with cell medium before loading was applied, so no on-chip liquid manipulation and DNA purification were needed. To validate its application for genetic analysis, Synechocystis PCC 6803 cells were loaded on the chip from 1000 cells to one cell per droplet, and their 16S rRNA gene (two copies per cell) was analyzed on a commercially available ABI StepOne real-time PCR thermal cycler. The result showed that the device is capable of genetic analysis at single bacterial cell level with C(q) standard deviation less than 1.05 cycles. The successful rate of this chip-based operation is more than 85% at the single bacterial cell level.
单细胞水平实时 PCR 是定量揭示同基因细胞异质性的不可或缺的工具。传统的利用微孔板或 PCR 管的 PCR 平台已被广泛应用,但它们的大反应体积不适合敏感的单细胞分析。微流控装置提供高密度、低体积的 PCR 室,但它们通常昂贵,需要专用设备来操纵液体和进行检测。为了解决这些限制,我们开发了一种廉价的芯片级设备,该设备与商业实时 PCR 热循环仪兼容,可用于单个细菌细胞的定量 PCR。该芯片包含 12 个表面附着的液滴,通过亲水图案定义,当它们浸入油中时,这些液滴充当实时 PCR 反应室。应用了一种一步法工艺,即在加载前将试剂与细胞培养基预混合,因此不需要在芯片上进行液体操作和 DNA 纯化。为了验证其在遗传分析中的应用,将 Synechocystis PCC 6803 细胞从 1000 个细胞加载到每个液滴一个细胞,并在市售的 ABI StepOne 实时 PCR 热循环仪上分析其 16S rRNA 基因(每个细胞两个拷贝)。结果表明,该设备能够以小于 1.05 个循环的 C(q)标准偏差进行单细胞水平的遗传分析。在单细胞水平上,该基于芯片的操作的成功率超过 85%。