State Key Laboratory Base of Novel Functional Materials and Preparation Science, Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211, PR China.
Faculty of Marine, Ningbo University, Ningbo 315211, PR China.
Biosens Bioelectron. 2016 Jan 15;75:308-14. doi: 10.1016/j.bios.2015.08.048. Epub 2015 Aug 28.
A novel multiplexed ratiometric biosensor array was fabricated on a homemade screen-printed carbon electrode (SPCE) for near-simultaneous detection of microRNA (miRNA)-21 and miRNA-141 based on electrochemiluminescence (ECL) coupled with cyclic voltammetry (CV) method. In the detection system, the ECL signal tags (Ru-SiO2@PLL-Au) were fabricated using poly-l-lysine (PLL) as bridging agent and co-reactant to connect Ru-SiO2 (Ru(bpy)3(2+)-doped silica) and gold nanoparticles (Au NPs), which were respectively modified on two spatial resolved working electrodes (WE1 and WE2) of SPCE. Then the ferrocene (Fc)-labeled hairpin DNA (Fc-HDNA1 and Fc-HDNA2) as CV signal tags and ECL quenching material were immobilized on Ru-SiO2@PLL-Au. Upon miRNA-21 and miRNA-141 adding, the target miRNAs could hybridize with corresponding Fc-HDNA, which could lead to Fc away from Ru-SiO2@PLL-Au. Such conformational changes could recover the ECL of Ru-SiO2@PLL-Au and decreased the CV current of Fc, respectively. This "signal-on" of ECL and "signal-off" of CV were employed for dual-signal ratiometric readout. With the help of a multiplexed switch, two dual-signals from WE1 and WE2 were used for multiplexed detection of miRNA-21 and miRNA-141 down to 6.3 and 8.6fM, respectively. This approach was used in real sample analysis and has significant potential for miRNA biomarkers detection in a clinical laboratory setting.
一种新型的多重比率生物传感器阵列是在自制的丝网印刷碳电极(SPCE)上制造的,用于基于电化学发光(ECL)与循环伏安法(CV)相结合的方法,对 microRNA(miRNA)-21 和 miRNA-141 进行近同时检测。在检测系统中,使用聚-L-赖氨酸(PLL)作为桥连剂和共反应物来连接电化学发光信号标记物(Ru-SiO2@PLL-Au),将 Ru-SiO2(Ru(bpy)3(2+)掺杂的二氧化硅)和金纳米粒子(Au NPs)分别修饰在 SPCE 的两个空间分辨工作电极(WE1 和 WE2)上。然后,将作为 CV 信号标记物和 ECL 猝灭材料的二茂铁(Fc)标记发夹 DNA(Fc-HDNA1 和 Fc-HDNA2)固定在 Ru-SiO2@PLL-Au 上。当添加 miRNA-21 和 miRNA-141 时,靶 miRNA 可以与相应的 Fc-HDNA 杂交,从而导致 Fc 远离 Ru-SiO2@PLL-Au。这种构象变化分别可以恢复 Ru-SiO2@PLL-Au 的 ECL 和降低 Fc 的 CV 电流。这种 ECL 的“信号开启”和 CV 的“信号关闭”被用于双信号比率读出。借助多路复用开关,从 WE1 和 WE2 获得的两个双信号用于分别对 miRNA-21 和 miRNA-141 进行多重检测,其检测限低至 6.3 和 8.6fM。该方法用于实际样品分析,在临床实验室环境中对 miRNA 生物标志物的检测具有重要的潜在应用价值。