Rezaei Meysam, Radfar Payar, Winter Marnie, McClements Lana, Thierry Benjamin, Warkiani Majid Ebrahimi
School of Biomedical Engineering, University of Technology Sydney, Sydney, New South Wales, 2007, Australia.
Institute for Biomedical Materials and Devices (IBMD), Faculty of Science, University of Technology Sydney, Sydney, New South Wales 2007, Australia.
Anal Chem. 2021 Mar 16;93(10):4584-4592. doi: 10.1021/acs.analchem.0c05026. Epub 2021 Mar 3.
Microfluidics-based technologies for single-cell analysis are becoming increasingly important tools in biological studies. With the increasing sophistication of microfluidics, cellular barcoding techniques, and next-generation sequencing, a more detailed picture of cellular subtype is emerging. Unfortunately, the majority of the methods developed for single-cell analysis are high-throughput and not suitable for rare cell analysis as they require a high input cell number. Here, we report a low-cost and reproducible method for rare single-cell analysis using a highly hydrophobic surface and nanosized static droplets. Our method allows rapid and efficient on-chip single-cell lysis and subsequent collection of genetic materials in nanoliter droplets using a micromanipulator or a laboratory pipette before subsequent genetic analysis. We show precise isolation of single cancer cells with high purity using two different strategies (i- cytospin and ii- static droplet array) for subsequent RNA analysis using droplet digital polymerase chain reaction (PCR) and real-time PCR. Our highly controlled isolation method opens a new avenue for the study of subcellular functional mechanisms, enabling the identification of rare cells of potential functional or pathogenic consequence.
基于微流控技术的单细胞分析方法正逐渐成为生物学研究中越来越重要的工具。随着微流控技术、细胞条形码技术和下一代测序技术的日益成熟,细胞亚型的更详细情况正在显现。不幸的是,大多数为单细胞分析开发的方法都是高通量的,不适合稀有细胞分析,因为它们需要大量的输入细胞数量。在此,我们报告一种低成本且可重复的方法,用于使用高度疏水表面和纳米级静态液滴进行稀有单细胞分析。我们的方法允许在随后的基因分析之前,使用显微操作器或实验室移液器在芯片上快速有效地进行单细胞裂解,并随后在纳升级液滴中收集遗传物质。我们展示了使用两种不同策略(i - 细胞涂片和ii - 静态液滴阵列)精确分离高纯度的单个癌细胞,以便随后使用液滴数字聚合酶链反应(PCR)和实时PCR进行RNA分析。我们高度可控的分离方法为亚细胞功能机制的研究开辟了一条新途径,能够识别具有潜在功能或致病后果的稀有细胞。