High-Throughput Microfluidic Single-Cell Digital Polymerase Chain Reaction

被引:74
|
作者
White, A. K. [1 ]
Heyries, K. A. [1 ]
Doolin, C. [2 ]
VanInsberghe, M. [1 ]
Hansen, C. L. [1 ,2 ]
机构
[1] Univ British Columbia, Ctr High Throughput Biol, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z4, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
HEMATOPOIETIC STEM-CELLS; MESSENGER-RNA; PCR; DNA; HETEROGENEITY; TRANSCRIPTOME; MICRORNAS; NUMBER; STATES;
D O I
10.1021/ac400896j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here we present an integrated microfluidic device for the high-throughput digital polymerase chain reaction (dPCR) analysis of single cells. This device allows for the parallel processing of single cells and executes all steps of analysis, including cell capture, washing, lysis, reverse transcription, and dPCR analysis. The cDNA from each single cell is distributed into a dedicated dPCR array consisting of 1020 chambers, each having a volume of 25 pL, using surface-tension-based sample partitioning. The high density of this dPCR format (118 900 chambers/cm(2)) allows the analysis of 200 single cells per run, for a total of 204 000 PCR reactions using a device footprint of 10 cm(2). Experiments using RNA dilutions show this device achieves shot-noise-limited performance in quantifying single molecules, with a dynamic range of 10(4). We performed over 1200 single-cell measurements, demonstrating the use of this platform in the absolute quantification of both high- and low-abundance mRNA transcripts, as well as micro-RNAs that are not easily measured using alternative hybridization methods. We further apply the specificity and sensitivity of single-cell dPCR to performing measurements of RNA editing events in single cells. High-throughput dPCR provides a new tool in the arsenal of single-cell analysis methods, with a unique combination of speed, precision, sensitivity, and specificity. We anticipate this approach will enable new studies where high-performance single-cell measurements are essential, including the analysis of transcriptional noise, allelic imbalance, and RNA processing.
引用
收藏
页码:7182 / 7190
页数:9
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