Guangdong Provincial Key Laboratory of Microbial Safety and Health, State Key Laboratory of Applied Microbiology Southern China, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou, 510070, People's Republic of China.
College of Food Science, South China Agricultural University, Guangzhou, 510642, People's Republic of China.
Mikrochim Acta. 2021 Aug 4;188(8):286. doi: 10.1007/s00604-021-04912-z.
A facile and versatile competitive electrochemical aptasensor for tobramycin (TOB) detection is described using electrochemical-deposited AuNPs coordinated with PEI-functionalized Fe-based metal-organic framework (AuNPs/P-MOF) as signal-amplification platform and a DNA probe labeled with methylene blue (MB) at the 3'-end (MB-Probe) as a signal producer. First, F-Probe (short complementary DNA strands of both the aptamer and the MB-Probe label with a sulfhydryl group at the 5'-end) was immobilized on the AuNPs/P-MOF modified electrode as detection probes, which competed with TOB in binding to the aptamer. TOB-aptamer binding resulted in F-Probe remaining unhybridized on the electrode surface, so that a significant current response was generated by hybridizing with MB-Probe instead. The developed strategy showed favorable repeatability, with a relative standard deviation (RSD) of 4.3% computed over five independent assays, and high stability, with only 6.8% degradation after 15 days of storage. Under optimal conditions, the proposed aptamer strategy exhibited a linear detection range from 100 pM to 500 nM with a limit of detection (LOD) of 56 pM (S/N = 3). The electrochemical aptasensor demonstrated remarkable selectivity, and its feasibility for accurate and quantitative detection of TOB in milk samples was confirmed (RSD < 4.5%). Due to its simple design, easy operation, and high sensitivity and selectivity, the proposed method could expect to detect other antibiotics by replacing the aptamers. In summary, this study provides a simple and effective new strategy for electrochemical aptasening based on MOF-based sensing interface. Scheme illustration of label-free competitive electrochemical aptamer-based detection of tobramycin based on electrochemically deposited AuNPs coordinated with PEI-functionalized Fe-based metal-organic framework as signal-amplification platform.
一种简单而通用的竞争电化学适体传感器,用于妥布霉素(TOB)的检测,使用电化学沉积的 AuNPs 与 PEI 功能化的 Fe 基金属有机骨架(AuNPs/P-MOF)作为信号放大平台,以及 3'端标记有亚甲基蓝(MB)的 DNA 探针(MB-Probe)作为信号产生物。首先,F-Probe(短互补 DNA 链,两端均带有巯基,其中一条包含适体,另一条包含 MB-Probe 标签)被固定在 AuNPs/P-MOF 修饰的电极上作为检测探针,与 TOB 竞争与适体结合。TOB-适体结合导致 F-Probe 留在电极表面上未杂交,因此通过与 MB-Probe 杂交产生了显著的电流响应。所开发的策略表现出良好的重复性,五个独立实验的相对标准偏差(RSD)为 4.3%,并且具有高稳定性,在 15 天的储存后仅降解 6.8%。在最佳条件下,该适体策略表现出从 100 pM 到 500 nM 的线性检测范围,检测限(LOD)为 56 pM(S/N = 3)。电化学适体传感器表现出显著的选择性,并证实了其在牛奶样品中准确和定量检测 TOB 的可行性(RSD < 4.5%)。由于其简单的设计、易于操作以及高灵敏度和选择性,该方法有望通过替换适体来检测其他抗生素。总之,本研究为基于 MOF 传感界面的无标记竞争电化学适体传感提供了一种简单有效的新策略。方案示意图:基于电化学沉积的 AuNPs 与 PEI 功能化的 Fe 基金属有机骨架作为信号放大平台,无标记竞争电化学适体法检测妥布霉素。