Kim Junsun, Jung Seungwon, Byoun Mun Sub, Yoo Changhoon, Sim Sang Jun, Lim Chae Seung, Kim Sung Woo, Kim Sang Kyung
Center for BioMicroSystems, Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, Seongbuk-gu, Korea.
Department of Chemical and Biological Engineering, Korea University, Seoul, Seongbuk-gu, Korea.
PLoS One. 2018 Jan 2;13(1):e0190451. doi: 10.1371/journal.pone.0190451. eCollection 2018.
Real-time PCR, also called quantitative PCR (qPCR), has been powerful analytical tool for detection of nucleic acids since it developed. Not only for biological research but also for diagnostic needs, qPCR technique requires capacity to detect multiple genes in recent years. Solid phase PCR (SP-PCR) where one or two directional primers are immobilized on solid substrates could analyze multiplex genetic targets. However, conventional SP-PCR was subjected to restriction of application for lack of PCR efficiency and quantitative resolution. Here we introduce an advanced qPCR with primer-incorporated network (PIN). One directional primers are immobilized in the porous hydrogel particle by covalent bond and the other direction of primers are temporarily immobilized at so-called 'Supplimers'. Supplimers released the primers to aqueous phase in the hydrogel at the thermal cycling of PCR. It induced the high PCR efficiency over 92% with high reliability. It reduced the formation of primer dimers and improved the selectivity of qPCR thanks to the strategy of 'right primers supplied to right place only'. By conducting a six-plex qPCR of 30 minutes, we analyzed DNA samples originated from malaria patients and successfully identified malaria species in a single reaction.
实时聚合酶链反应(Real-time PCR),也称为定量聚合酶链反应(qPCR),自其发展以来一直是检测核酸的强大分析工具。近年来,不仅出于生物学研究目的,而且为了满足诊断需求,qPCR技术需要具备检测多个基因的能力。固相聚合酶链反应(SP-PCR),即将一或两个定向引物固定在固体基质上,能够分析多个遗传靶点。然而,传统的SP-PCR由于缺乏PCR效率和定量分辨率而受到应用限制。在此,我们介绍一种先进的带有引物掺入网络(PIN)的qPCR。一个定向引物通过共价键固定在多孔水凝胶颗粒中,另一个方向的引物暂时固定在所谓的“补充引物(Supplimers)”上。在PCR热循环过程中,补充引物将引物释放到水凝胶中的水相中。这使得PCR效率高达92%以上,且可靠性高。由于采用了“仅将正确的引物供应到正确的位置”这一策略,它减少了引物二聚体的形成,并提高了qPCR的选择性。通过进行30分钟的六重qPCR,我们分析了源自疟疾患者的DNA样本,并在单一反应中成功鉴定出疟原虫种类。