Nanobiosensors Lab, Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
Department of Nanotechnology, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
Mikrochim Acta. 2022 Sep;189(9):357. doi: 10.1007/s00604-022-05455-7. Epub 2022 Aug 30.
Rapid and sensitive detection of biomarkers enables monitoring patients' health status and can enhance the early diagnosis of deadly diseases. In this work, we have developed a new colorimetric platform based on spherical nucleic acid (SNA) and G-quadruplex DNAzymes for the identification of specific miRNAs. The simple hybridization between the target miRNA and two capture probes (capture probe 1 located at AuNP surface and free capture probe 2) is the working principle of this biosensor. The hybridization and duplex formation among probes and miRNAs led to a significant decrease in the intensity of color change. A linear relationship between the decrease of colorimetric signal and the amount of target molecules was witnessed from 1 to 100 nM for miRNA-155. Using this method, we were able to detect concentrations of miRNA-155 as low as 0.7 nM. Furthermore, the proposed sensing platform can be utilized profitably to detect miRNA-155 in real human serum samples. We further investigated the applicability of the proposed method in a microfluidic system which displayed promising results. In this project, A G-quadruplex based SNAzyme was constructed to provide a fast and simple colorimetric method for miRNA detection. The SNAzyme actually employed as both target recognition element and catalytic nano labels for colorimetric detection.
快速灵敏地检测生物标志物可以监测患者的健康状况,并能增强对致命疾病的早期诊断。在这项工作中,我们开发了一种基于球形核酸(SNA)和 G-四链体 DNA 酶的新比色平台,用于鉴定特定的 miRNA。该生物传感器的工作原理是目标 miRNA 与两个捕获探针(位于 AuNP 表面的捕获探针 1 和游离捕获探针 2)之间的简单杂交。探针和 miRNA 之间的杂交和双链体形成导致颜色变化强度显著降低。从 1 到 100 nM 的 miRNA-155 见证了比色信号减少与目标分子数量之间的线性关系。使用这种方法,我们能够检测到低至 0.7 nM 的 miRNA-155 浓度。此外,所提出的传感平台可用于在真实的人血清样本中检测 miRNA-155。我们进一步研究了该方法在微流控系统中的适用性,结果显示出有前景的结果。在这个项目中,构建了基于 G-四链体的 SNAzyme,为 miRNA 检测提供了一种快速简单的比色方法。SNAzyme 实际上既用作靶识别元件,也用作比色检测的催化纳米标签。