Liu Gang, Wan Ying, Gau Vincent, Zhang Jiong, Wang Lihua, Song Shiping, Fan Chunhai
Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.
J Am Chem Soc. 2008 May 28;130(21):6820-5. doi: 10.1021/ja800554t. Epub 2008 May 7.
In this work, we report an enzyme-based E-DNA sensor for the sequence-specific detection of nucleic acids. This DNA sensor employs a "stem-loop" DNA probe dually labeled with biotin and digoxigenin (DIG). The probe is immobilized at an avidin-modified electrode surface via the biotin-avidin bridge, and the DIG serves as an affinity tag for the enzyme binding. In the initial state of the sensor, the probe adopts the stem-loop structure, which shields DIG from being approached by a bulky horseradish peroxidase-linked-anti-DIG antibody (anti-DIG-HRP) due to the steric effect. After hybridization, the probe undergoes a significant conformational change, forcing DIG away from the electrode. As a result, the DIG label becomes accessible by the anti-DIG-HRP, and the target hybridization event can be sensitively transduced via the enzymatically amplified electrochemical current signal. By using this new strategy, we demonstrate that the prototype E-DNA sensor has been able to detect as low as femtomolar DNA targets with excellent differentiation ability for even single mismatches.
在这项工作中,我们报道了一种基于酶的E-DNA传感器,用于核酸的序列特异性检测。这种DNA传感器采用了一种双标记有生物素和地高辛(DIG)的“茎环”DNA探针。该探针通过生物素-抗生物素蛋白桥固定在抗生物素蛋白修饰的电极表面,DIG作为酶结合的亲和标签。在传感器的初始状态下,探针采用茎环结构,由于空间位阻效应,该结构可保护DIG不被体积较大的辣根过氧化物酶标记的抗DIG抗体(抗DIG-HRP)接近。杂交后,探针发生显著的构象变化,迫使DIG远离电极。结果,DIG标签可被抗DIG-HRP识别,并且可以通过酶促放大的电化学电流信号灵敏地转导目标杂交事件。通过使用这种新策略,我们证明了原型E-DNA传感器能够检测低至飞摩尔浓度的DNA靶标,并且对单个错配具有出色的区分能力。