Si Yanmei, Xu Lan, Deng Ting, Zheng Jing, Li Jishan
Institute of Applied Chemistry, School of Science, Central South University of Forestry and Technology, Changsha 410004, P. R. China.
Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063, P. R. China.
ACS Sens. 2020 Dec 24;5(12):4009-4016. doi: 10.1021/acssensors.0c01876. Epub 2020 Dec 7.
The abnormal expression of some miRNAs is often closely related to the development of tumors. Available detection methods or biosensors that can simultaneously quantify multiple miRNAs in a single sample have rarely been reported. Herein, a novel catalytic hairpin self-assembly (CHA)-based surface-enhanced Raman scattering (SERS) sensor array was developed to simultaneously measure multiple miRNAs associated with cancer in one sample. The sensor array with four different sensing units was constructed by immobilizing one of four different hairpin-structured DNA sequence 1 (hp1) onto one of four Au/Ag alloy nanoparticle (AuAgNP)-coated detection wells. When target miRNA is present, the SERS tags, which were prepared by modifying AuAgNPs with a Raman reporter molecule of 4-mercaptobenzonitrile (MPBN) and the related hairpin-structured DNA sequence 2 (hp2), were captured onto the corresponding sensor unit through a repeated specific CHA reaction. This generated many "hot spots" because of interactions between the SERS tags and the AuAgNP layer-coated surface of the sensor, which ultimately produced a strong SERS signal that allowed the detection of target miRNAs with the detection limit of 0.15 pM. Using this SERS sensor array, multiple cancer-associated miRNAs (miR-1246, miR-221, miR-133a, and miR-21) were successfully determined in buffer, serum, and cellular RNA extracts.
一些微小RNA(miRNA)的异常表达通常与肿瘤的发生发展密切相关。目前很少有报道能够在单个样本中同时定量多种miRNA的检测方法或生物传感器。在此,我们开发了一种基于新型催化发夹自组装(CHA)的表面增强拉曼散射(SERS)传感器阵列,用于在一个样本中同时检测多种与癌症相关的miRNA。通过将四种不同的发夹结构DNA序列1(hp1)之一固定在四个金/银合金纳米颗粒(AuAgNP)包覆的检测孔之一上,构建了具有四个不同传感单元的传感器阵列。当存在目标miRNA时,通过用4-巯基苯甲腈(MPBN)的拉曼报告分子和相关的发夹结构DNA序列2(hp2)修饰AuAgNP制备的SERS标签,通过重复的特异性CHA反应被捕获到相应的传感器单元上。由于SERS标签与传感器的AuAgNP层包覆表面之间的相互作用,产生了许多“热点”,最终产生了强烈的SERS信号,使得能够以0.15 pM的检测限检测目标miRNA。使用这种SERS传感器阵列,成功地在缓冲液、血清和细胞RNA提取物中测定了多种与癌症相关的miRNA(miR-1246、miR-221、miR-133a和miR-21)。