Oishi Motoi
Division of Materials Science, Faculty of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8573, Japan.
ACS Omega. 2018 Mar 31;3(3):3321-3329. doi: 10.1021/acsomega.7b01866. Epub 2018 Mar 20.
Because circulating microRNAs (miRNAs) have been recognized as a new class of blood-based biomarkers for various diseases, a significant challenge has been the development of point-of-care testing (POCT) systems based on detection of circulating miRNAs directly from serum. A promising approach to POCT systems is considered to be the development of enzyme-free and isothermal detection systems. Here, two types of DNA circuit system based on proportional and exponential amplification strategies were constructed using double-stranded DNA-modified magnetic beads (dsDNA-MBs) and their performances for detection of miRNA were studied comparatively. Both proportional and exponential amplification DNA circuit systems enabled the detection of target miRNA (miR-141) at room temperature without the need for additional enzymes because miR-141 acted as a catalyst for successive toehold-mediated DNA displacement reactions. A significant increase in the noise fluorescence signal was observed for the exponential amplification DNA circuit system because of the leakage (undesired DNA displacement reaction) revealed by the kinetic study on each DNA displacement reaction. Nevertheless, the exponential amplification DNA circuit system showed a lower limit of detection (LOD: 46 pM) and shorter assay time (15 min) compared to those of the proportional amplification DNA circuit system (LOD: 103 pM at 180 min). It is most likely that the exponential amplification DNA circuit system enabled amplification of both the signals and target miR-141, whereas the proportional amplification DNA circuit system enabled amplification of the signals alone. In addition, the exponential amplification DNA circuit system was able to discriminate between mismatched base sequences in miR-200 family members and specifically detect miR-141 even in the presence of serum. These findings are important for the rational design for POCT systems.
由于循环微RNA(miRNA)已被公认为各类疾病基于血液的新型生物标志物,因此一个重大挑战是开发基于直接从血清中检测循环miRNA的即时检测(POCT)系统。POCT系统的一种有前景的方法被认为是开发无酶等温检测系统。在此,使用双链DNA修饰的磁珠(dsDNA-MB)构建了基于比例和指数扩增策略的两种DNA电路系统,并对其检测miRNA的性能进行了比较研究。比例和指数扩增DNA电路系统都能够在室温下检测目标miRNA(miR-141),无需额外的酶,因为miR-141充当了连续的链置换介导的DNA置换反应的催化剂。由于对每个DNA置换反应的动力学研究揭示的泄漏(不期望的DNA置换反应),指数扩增DNA电路系统的噪声荧光信号显著增加。然而,与比例扩增DNA电路系统(180分钟时的检测限为103 pM)相比,指数扩增DNA电路系统显示出更低的检测限(LOD:46 pM)和更短的检测时间(15分钟)。很可能指数扩增DNA电路系统能够同时扩增信号和目标miR-141,而比例扩增DNA电路系统只能扩增信号。此外,指数扩增DNA电路系统能够区分miR-200家族成员中的错配碱基序列,甚至在存在血清的情况下也能特异性检测miR-141。这些发现对于POCT系统的合理设计很重要。