Jung Seungwon, Kim Junsun, Lee Dong Jin, Oh Eun Hae, Lim Hwasup, Kim Kwang Pyo, Choi Nakwon, Kim Tae Song, Kim Sang Kyung
Center for BioMicrosystems, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, Korea.
Department of Chemical &Biological Engineering, Korea University, Seoul, Korea.
Sci Rep. 2016 Mar 11;6:22975. doi: 10.1038/srep22975.
Multiplex quantitative real-time PCR (qPCR), which measures multiple DNAs in a given sample, has received significant attention as a mean of verifying the rapidly increasing genetic targets of interest in single phenotype. Here we suggest a readily extensible qPCR for the expression analysis of multiple microRNA (miRNA) targets using microparticles of primer-immobilized networks as discrete reactors. Individual particles, 200~500 μm in diameter, are identified by two-dimensional codes engraved into the particles and the non-fluorescent encoding allows high-fidelity acquisition of signal in real-time PCR. During the course of PCR, the amplicons accumulate in the volume of the particles with high reliability and amplification efficiency over 95%. In a quick assay comprising of tens of particles holding different primers, each particle brings the independent real-time amplification curve representing the quantitative information of each target. Limited amount of sample was analyzed simultaneously in single chamber through this highly multiplexed qPCR; 10 kinds of miRNAs from purified extracellular vesicles (EVs).
多重定量实时聚合酶链反应(qPCR)可在给定样本中检测多种DNA,作为验证单表型中快速增加的感兴趣基因靶点的一种手段,它受到了广泛关注。在此,我们提出一种易于扩展的qPCR方法,用于使用固定引物网络的微粒作为离散反应器来分析多个微小RNA(miRNA)靶点的表达。直径为200~500μm的单个微粒通过刻在微粒上的二维编码进行识别,这种非荧光编码允许在实时PCR中高保真地获取信号。在PCR过程中,扩增子以高可靠性在微粒体积中积累,扩增效率超过95%。在由持有不同引物的数十个微粒组成的快速检测中,每个微粒都带来独立的实时扩增曲线,代表每个靶点的定量信息。通过这种高度多重的qPCR,在单个反应室中可同时分析有限量的样本;从纯化的细胞外囊泡(EV)中检测10种miRNA。