Tang Danyao, Xiong Chunyuan, Wu YeYu, Luo Hu, Yan Jun, Huang Ke-Jing, Tan Xuecai, Ya Yu
Education Department of Guangxi Zhuang Autonomous Region, Laboratory of Optic-electric Chemo/Biosensing and Molecular Recognition, Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning, 530006, China.
Education Department of Guangxi Zhuang Autonomous Region, Laboratory of Optic-electric Chemo/Biosensing and Molecular Recognition, Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning, 530006, China.
Talanta. 2025 Apr 1;285:127321. doi: 10.1016/j.talanta.2024.127321. Epub 2024 Dec 2.
This paper presents a self-powered biosensing platform based on graphdiyne@Au (2D GDY@Au) nanoparticles and rolling circle-hybridization chain (RC-HC) dual linear cascade amplification technology, which significantly enhances target recognition and signal amplification efficiency for miRNA-141. Specifically, the target on bioanode outputs a large amount of single-stranded DNA (T1) through the strand displacement amplification (SDA) mechanism. This efficient target recycling process triggers RC-HC dual linear cascade reaction. The RCA product and H2 form the L-Liner/H2 hybridized chain through a hybridization chain reaction, and then are immobilized on a flexible electrode using a Y-DNA capture handle. [Ru(NH)] is precisely anchored in the grooves of the DNA double helix. The 2D GDY@Au enhances the electron mobility of the system to form a rich electron-donating center. The [Ru(NH)] on the biocathode receives electrons and is reduced to [Ru(NH)], producing a significantly amplified open-circuit voltage signal. Dual linear cascade amplification technology realizes precise target recognition, exponential amplification, and efficient conversion of biological signals. This technique displays an extensive linear range (0.0001-10000 pM) with a detection limit of 25.9 aM (S/N = 3), and it provides an innovative method for developing sensors based on nucleic acid amplification and presents a promising novel approach for the sensitive and precise detection of low-abundance target molecules, highlighting a new tactic for the creation of compact and portable analytical devices.
本文提出了一种基于石墨炔@金(二维石墨炔@金)纳米颗粒和滚环杂交链(RC-HC)双线性级联放大技术的自供电生物传感平台,该平台显著提高了对miRNA-141的靶标识别和信号放大效率。具体而言,生物阳极上的靶标通过链置换扩增(SDA)机制输出大量单链DNA(T1)。这种高效的靶标循环过程触发了RC-HC双线性级联反应。滚环扩增(RCA)产物与H2通过杂交链反应形成L-Liner/H2杂交链,然后使用Y-DNA捕获手柄固定在柔性电极上。[Ru(NH)]精确锚定在DNA双螺旋的凹槽中。二维石墨炔@金增强了系统的电子迁移率,形成了丰富的电子供体中心。生物阴极上的[Ru(NH)]接收电子并被还原为[Ru(NH)],产生显著放大的开路电压信号。双线性级联放大技术实现了精确的靶标识别、指数放大和生物信号的高效转换。该技术显示出广泛的线性范围(0.0001-10000 pM),检测限为25.9 aM(S/N = 3),为基于核酸扩增的传感器开发提供了一种创新方法,为低丰度靶标分子的灵敏精确检测提供了一种有前景的新方法,突出了创建紧凑便携式分析设备的新策略。