College of Chemistry and Life Science, Zhejiang Normal University, Jinhua, 321004, PR China; Jiaxing Key Laboratory of Molecular Recognition and Sensing, College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, 314001, PR China.
Department of Pathology, First Hospital of Jiaxing, Affiliated Hospital of Jiaxing University, Jiaxing, 314000, PR China.
Talanta. 2023 Aug 1;260:124646. doi: 10.1016/j.talanta.2023.124646. Epub 2023 May 5.
Heterogeneous electrochemical DNA biosensors have attracted huge attention due to their enhanced signal sensitivity, compared to homogeneous biosensors. However, the high cost of probe labeling and the reduced recognition efficiency associated with current heterogeneous electrochemical biosensors confine their potential applications. In the present work, a dual-blocker assisted and dual-label-free heterogeneous electrochemical strategy based on multi-branched hybridization chain reaction (mbHCR) and reduced graphene oxide (rGO) was fabricated for ultrasensitive detection of DNA. The target DNA could trigger the mbHCR of two DNA hairpin probes, resulting in the generation of multi-branched long chain of DNA duplexes with bidirectional arms. One direction of the multi-branched arms in the mbHCR products were then bound to the label-free capture probe on the gold electrode through multivalent hybridization with enhanced recognition efficiency. The other direction of multi-branched arms in mbHCR product could adsorb rGO via π-π stacking interactions. Two DNA blockers were ingeniously designed to block the binding of excessive H1-pAT on electrode and to prevent the adsorption of rGO by residual unbound capture probes. As a result, with the electrochemical reporter methylene blue selectively intercalated into the long chain of DNA duplex and absorbed on rGO, a remarkable electrochemical signal rise was observed. Thus, a dual-blocker aided and dual-label-free electrochemical strategy for ultrasensitive DNA detection is readily realized with the merit of cost-effective. The as-developed dual-label-free electrochemical biosensor has great potential to be employed in nucleic acid related medical diagnostics.
由于其信号灵敏度增强,与均相生物传感器相比,异质电化学 DNA 生物传感器引起了人们的极大关注。然而,当前异质电化学生物传感器中探针标记的高成本和识别效率的降低限制了它们的潜在应用。在本工作中,基于多分支杂交链式反应(mbHCR)和还原氧化石墨烯(rGO)构建了一种双阻断剂辅助和双无标记的异质电化学策略,用于超灵敏检测 DNA。目标 DNA 可以触发两个 DNA 发夹探针的 mbHCR,从而产生具有双向臂的 DNA 双链的多分支长链。mbHCR 产物中的多分支臂的一个方向通过多价杂交与金电极上的无标记捕获探针结合,从而提高了识别效率。mbHCR 产物中的多分支臂的另一个方向可以通过 π-π 堆积相互作用吸附 rGO。巧妙地设计了两个 DNA 阻断剂来阻止过量 H1-pAT 在电极上的结合,并防止 rGO 通过残留的未结合捕获探针吸附。结果,电化学报告分子亚甲基蓝选择性地嵌入 DNA 双链的长链中并吸附在 rGO 上,观察到显著的电化学信号上升。因此,通过成本效益高的优点,实现了一种双阻断剂辅助和双无标记电化学策略用于超灵敏 DNA 检测。所开发的无标记电化学生物传感器在核酸相关医学诊断中具有很大的应用潜力。