Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, Ministry of Education; Shandong Key Laboratory of Biochemical Analysis; Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong; College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China.
Anal Chem. 2021 Aug 3;93(30):10679-10687. doi: 10.1021/acs.analchem.1c02186. Epub 2021 Jul 21.
Herein, an electrochemiluminescence (ECL) microRNA biosensor based on anti-fouling magnetic beads (MBs) and two signal amplification strategies was developed. The newly designed anti-fouling dendritic peptide was wrapped on the surfaces of MBs to make them resistant to nonspecific adsorption of biomolecules in complex biological samples so as to realize accurate and selective target recognition. One of the amplification strategies was achieved through nucleic acid cycle amplification based on the DNAzyme on the surfaces of MBs. Then, the output DNA generated by the nucleic acid cycle amplification program stimulated the hybrid chain reaction (HCR) process on the modified electrode surface to generate the other amplification of the ECL response. Titanium dioxide nanoneedles (TiO NNs), as a co-reaction accelerator of the Ru(bpy)(cpaphen) and tripropylamine (TPrA) system, were wrapped with the electrodeposited polyaniline (PANI) on the electrode surface to enhance the ECL intensity of Ru(bpy)(cpaphen). The conducting polymer PANI can not only immobilize the TiO NNs but also improve the conductivity of the modified electrodes. The biosensor exhibited ultra-high sensitivity and excellent selectivity toward the detection of miRNA 21, with a detection limit of 0.13 fM. More importantly, with the anti-fouling MBs as a unique separation tool, this ECL biosensor was capable of assaying targets in complex biological media such as serum and cell lysate.
本文构建了一种基于抗污磁珠(MBs)和两种信号放大策略的电化学发光(ECL)microRNA 生物传感器。新设计的抗污树枝状肽被包裹在 MBs 表面,使它们能够抵抗复杂生物样品中生物分子的非特异性吸附,从而实现对靶标的准确和选择性识别。其中一种放大策略是基于 MBs 表面的 DNA 酶实现核酸循环扩增。然后,核酸循环扩增方案产生的输出 DNA 可刺激修饰电极表面上的杂交链式反应(HCR)过程,从而产生 ECL 响应的另一种放大。作为 Ru(bpy)(cpaphen)和三丙胺(TPrA)体系的共反应加速剂,二氧化钛纳米针(TiO NNs)被包裹在电极表面上电沉积的聚苯胺(PANI)上,以增强 Ru(bpy)(cpaphen)的 ECL 强度。导电聚合物 PANI 不仅可以固定 TiO NNs,还可以提高修饰电极的导电性。该生物传感器对 miRNA 21 的检测具有超高的灵敏度和出色的选择性,检测限低至 0.13 fM。更重要的是,该 ECL 生物传感器采用抗污 MBs 作为独特的分离工具,能够在血清和细胞裂解液等复杂生物介质中检测靶标。