Suppr超能文献

基于 G-四链体 DNA 酶修饰的球形核酸的 miRNA-155 灵敏比色检测

Sensitive colorimetric detection of miRNA-155 via G-quadruplex DNAzyme decorated spherical nucleic acid.

机构信息

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.

出版信息

Mikrochim Acta. 2022 Sep;189(9):357. doi: 10.1007/s00604-022-05455-7. Epub 2022 Aug 30.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验