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基于电化学双适体的生物传感器,通过纳米杂化电催化剂标记与 DNA 纳米四面体结构的结合,实现对心肌肌钙蛋白 I 的非酶检测。

Electrochemical dual-aptamer-based biosensor for nonenzymatic detection of cardiac troponin I by nanohybrid electrocatalysts labeling combined with DNA nanotetrahedron structure.

机构信息

Center for Drug Research and Development, Guangdong Pharmaceutical University, Guangzhou, 510006, China; Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems, Guangdong Pharmaceutical University, Guangzhou, 510006, China; Key Laboratory of New Drug Discovery and Evaluation of Ordinary Universities of Guangdong Province, Guangdong Pharmaceutical University, Guangzhou, 510006, China; School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, 510006, China.

School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, 510006, China.

出版信息

Biosens Bioelectron. 2019 Jun 1;134:49-56. doi: 10.1016/j.bios.2019.03.049. Epub 2019 Mar 29.

Abstract

The accurate detection of biomarkers for acute myocardial infarction (AMI) plays an important role in clinical diagnosis and management process. In this work, we developed an electrochemical biosensor by using magnetic metal organic framework (MMOF) nanocatalysts and DNA nanotetrahedron (NTH) based dual-aptamer probes for nonenzymatic detection of cardiac troponin I (cTnI), a gold standard biomarker for the early diagnosis of AMI. Firstly, the NTH-assisted dual-aptamer (Tro4 and Tro6) capture probes were immobilized on the screen-printed gold electrode (SPGE) for the highly enhanced capture the target cTnI with steady support and optimized interface density. Then, the MMOF FeO@UiO-66 nanozymes were decorated by bimetallic Cu@Au nanoparticles and two kinds of aptamer. This fabricated nonenzymatic nanoprobe1 (NP1) can be applied for recognizing the cTnI specifically and amplifying the current signal by catalyzing the oxidation of hydroquinone (HQ) to benzoquinone (BQ) with HO. The target proteins were captured to fabricate a supersandwich-like structure on a SPGE interface. Furthermore, the nanoprobe2 (NP2) of Cu@Au nanozymes labeled with dual-complementary DNA (cDNA) to the dual-aptamer, were anchored on the NP1 through DNA hybridization, leading to the formation of cluster-based nanoprobes for further enhancing detection sensitivity. Finally, this enzyme-free electrochemical aptasensor exhibited great analytical performance with a dynamic range of 0.05-100 ng/mL, a low detection limit of 16 pg/mL, high selectivity and good repeatability. The fabricated aptasensor has great potential development in the field of clinic disease diagnostics for AMI.

摘要

急性心肌梗死 (AMI) 标志物的准确检测在临床诊断和管理过程中起着重要作用。在这项工作中,我们开发了一种电化学生物传感器,该传感器使用磁性金属有机骨架 (MMOF) 纳米催化剂和基于 DNA 纳米四面体 (NTH) 的双适体探针,用于非酶检测心脏肌钙蛋白 I (cTnI),这是 AMI 早期诊断的金标准生物标志物。首先,NTH 辅助的双适体 (Tro4 和 Tro6) 捕获探针被固定在丝网印刷金电极 (SPGE) 上,用于高度增强捕获目标 cTnI,具有稳定的支撑和优化的界面密度。然后,通过双金属 Cu@Au 纳米粒子和两种适体修饰 MMOF FeO@UiO-66 纳米酶。所制备的非酶纳米探针 1 (NP1) 可特异性识别 cTnI,并通过催化 HQ 氧化为 BQ 与 HO 放大电流信号。目标蛋白被捕获到 SPGE 界面上形成超三明治样结构。此外,带有双互补 DNA (cDNA) 的 Cu@Au 纳米酶标记的纳米探针 2 (NP2) 与双适体结合,通过 DNA 杂交锚定在 NP1 上,导致基于簇的纳米探针形成,进一步提高检测灵敏度。最后,这种无酶电化学适体传感器表现出优异的分析性能,具有 0.05-100ng/mL 的动态范围、16pg/mL 的低检测限、高选择性和良好的重复性。所制备的适体传感器在 AMI 临床疾病诊断领域具有很大的潜在发展前景。

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