Single cell digital polymerase chain reaction on self-priming compartmentalization chip

• Published in: Biomicrofluidics Vol. 11; no. 1; p. 014109
• Main Authors: Zhu, Qiangyuan, Qiu, Lin, Xu, Yanan, Li, Guang, Mu, Ying
• Format: Journal Article
• Language: English
• Published: United States American Institute of Physics 01.01.2017; AIP Publishing LLC
• Subjects: Biology; Coefficient of variation; Deoxyribonucleic acid; Digitization; DNA; Gene expression; Polymerase chain reaction; Priming; Reagents; Regular; Reproducibility; Sensitivity analysis
• ISSN: 1932-1058; 1932-1058
• DOI: 10.1063/1.4975192

Single cell analysis provides a new framework for understanding biology and disease, however, an absolute quantification of single cell gene expression still faces many challenges. Microfluidic digital polymerase chain reaction (PCR) provides a unique method to absolutely quantify the single cell gene expression, but only limited devices are developed to analyze a single cell with detection variation. This paper describes a self-priming compartmentalization (SPC) microfluidic digital polymerase chain reaction chip being capable of performing single molecule amplification from single cell. The chip can be used to detect four single cells simultaneously with 85% of sample digitization. With the optimized protocol for the SPC chip, we first tested the ability, precision, and sensitivity of our SPC digital PCR chip by assessing β-actin DNA gene expression in 1, 10, 100, and 1000 cells. And the reproducibility of the SPC chip is evaluated by testing 18S rRNA of single cells with 1.6%–4.6% of coefficient of variation. At last, by detecting the lung cancer related genes, PLAU gene expression of A549 cells at the single cell level, the single cell heterogeneity was demonstrated. So, with the power-free, valve-free SPC chip, the gene copy number of single cells can be quantified absolutely with higher sensitivity, reduced labor time, and reagent. We expect that this chip will enable new studies for biology and disease.