State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210023 , People's Republic of China.
Anal Chem. 2018 Apr 17;90(8):5503-5508. doi: 10.1021/acs.analchem.8b01217. Epub 2018 Apr 6.
A bipedal molecular machine powered surface programmatic chain reaction was designed for electrochemical signal amplification and highly sensitive electrochemical detection of protein. The bipedal molecular machine was built through aptamer-target specific recognition for the binding of one target protein with two DNA probes, which hybridized with surface-tethered hairpin DNA 1 (H1) via proximity effect to expose the prelocked toehold domain of H1 for the hybridization of ferrocene-labeled hairpin DNA 2 (H2-Fc). The toehold-mediated strand displacement reaction brought the electrochemical signal molecule Fc close to the electrode and meanwhile released the bipedal molecular machine to traverse the sensing surface by the surface programmatic chain reaction. Eventually, a large number of duplex structures of H1-H2 with ferrocene groups facing to the electrode were formed on the sensor surface to generate an amplified electrochemical signal. Using thrombin as a model target, this method showed a linear detection range from 2 pM to 20 nM with a detection limit of 0.76 pM. The proposed detection strategy was enzyme-free and allowed highly sensitive and selective detection of a variety of protein targets by using corresponding DNA-based affinity probes, showing potential application in bioanalysis.
一种基于双足分子机器的表面程序化链式反应被设计用于电化学生物传感器信号的放大和蛋白质的高灵敏电化学检测。双足分子机器通过适体-靶标特异性识别,两个 DNA 探针与一个靶标蛋白结合,通过近邻效应使 DNA 探针 1(H1)杂交,暴露出 H1 的预锁定的连接臂区域,用于与二茂铁标记的发夹 DNA 2(H2-Fc)杂交。引发链置换反应使电化学信号分子 Fc 靠近电极,同时通过表面程序化链式反应释放双足分子机器在传感表面上迁移。最终,在传感器表面形成了大量具有电化学活性的二茂铁基团面向电极的 H1-H2 双链结构,从而产生放大的电化学生物传感器信号。该方法以凝血酶为模型靶标,检测范围从 2 pM 至 20 nM,检测限为 0.76 pM。该检测策略无需酶,通过使用相应的基于 DNA 的亲和探针,实现了对多种蛋白质靶标的高灵敏和选择性检测,在生物分析中具有潜在的应用前景。