Zhang Jing, Qi Honglan, Li Yan, Yang Jia, Gao Qiang, Zhang Chengxiao
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Materials Science, Shaanxi Normal University, Xi'an 710062, China.
Anal Chem. 2008 Apr 15;80(8):2888-94. doi: 10.1021/ac701995g. Epub 2008 Mar 14.
A highly selective electrogenerated chemiluminescence (ECL) biosensor for the detection of target single-strand DNA (ss-DNA) was developed using hairpin DNA as the recognition element and ruthenium complex as the signal-producing compound. The ECL-based DNA biosensor was fabricated by self-assembling the ECL probe of thiolated hairpin DNA tagged with ruthenium complex on the surface of a gold electrode. In the absence of target ss-DNA, the ECL probe immobilized on the surface of the electrode was in the folded configuration in which its termini were held in close proximity to the electrode, and thus a strong ECL signal could be generated. In the presence of target ss-DNA, a stem-loop of the ECL probe on the electrode was converted into a linear double-helix configuration due to hybridization, resulting in the tag moving away from the electrode surface, which in turn decreased the ECL signal. The ECL intensity of the DNA biosensor generated a "switch off" mode, which decreased with an increase of the concentration of target DNA, and a detection limit of 9 x 10(-11) M complementary target ss-DNA was achieved. Single mismatched target ss-DNA was effectively discriminated from complementary target ss-DNA. The effect of different loop lengths of the hairpin DNA on the selectivity of the ECL DNA biosensor has been investigated. This work demonstrated that the sensitivity and specificity of an ECL DNA biosensor could be greatly improved using a hairpin DNA species which has an appropriate stem and loop length as the recognition element.
一种用于检测目标单链DNA(ss-DNA)的高选择性电化学发光(ECL)生物传感器被开发出来,该传感器使用发夹DNA作为识别元件,钌配合物作为信号产生化合物。基于ECL的DNA生物传感器是通过将标记有钌配合物的硫醇化发夹DNA的ECL探针自组装在金电极表面而制备的。在没有目标ss-DNA的情况下,固定在电极表面的ECL探针处于折叠构型,其末端靠近电极,因此可以产生强烈的ECL信号。在存在目标ss-DNA的情况下,由于杂交,电极上ECL探针的茎环结构转变为线性双螺旋构型,导致标记物远离电极表面,进而降低了ECL信号。DNA生物传感器的ECL强度呈现“关闭”模式,随着目标DNA浓度的增加而降低,实现了对互补目标ss-DNA的检测限为9×10⁻¹¹ M。单碱基错配的目标ss-DNA能够与互补目标ss-DNA有效区分。研究了发夹DNA不同环长度对ECL DNA生物传感器选择性的影响。这项工作表明,使用具有合适茎和环长度的发夹DNA物种作为识别元件,可以大大提高ECL DNA生物传感器的灵敏度和特异性。