State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
Biosens Bioelectron. 2017 Jan 15;87:732-736. doi: 10.1016/j.bios.2016.09.036. Epub 2016 Sep 12.
In this work, a simple, signal-on and label-free electrochemical biosensor for ultrasensitive DNA detection is reported on the basis of an autocatalytic and exonuclease III (Exo III)-assisted cascade signal amplification strategy. In the presence of target DNA (T-DNA), the hybridization between the 3'-protruding DNA fragment of hairpin DNA probe (HP1) and T-DNA triggered the Exo III cleavage process, accompanied by the releasing of T-DNA and autonomous generation of new DNA fragment which was used for the successive hybridization with the another hairpin DNA (HP2) on the electrode. After the Exo III cleavage process, numerous quadruplex-forming oligomers which caged in HP2 were liberated on the electrode surface and folded into G-quadruplex-hemin complexes with the help of K and hemin to give a remarkable electrochemical response. As a result, a low detection limit of 4.83fM with an excellent selectivity toward T-DNA was achieved. The developed electrochemical biosensor should be further extended for the detection of a wide spectrum of analytes and has great potential for the development of ultrasensitive biosensing platform for early diagnosis in gene-related diseases.
在这项工作中,基于自动催化和外切酶 III(Exo III)辅助级联信号放大策略,报道了一种用于超灵敏 DNA 检测的简单、信号开启和无标记的电化学生物传感器。在存在靶 DNA(T-DNA)的情况下,发夹 DNA 探针(HP1)的 3'-突出 DNA 片段与 T-DNA 之间的杂交触发了 Exo III 切割过程,伴随着 T-DNA 的释放和新 DNA 片段的自主生成,该片段用于与电极上的另一个发夹 DNA(HP2)的连续杂交。在 Exo III 切割过程之后,大量在 HP2 中被笼困住的四链体形成寡聚物在电极表面上被释放出来,并在 K 和血红素的帮助下折叠成 G-四链体-血红素复合物,从而产生显著的电化学响应。结果,实现了低至 4.83fM 的检测限,并且对 T-DNA 具有优异的选择性。开发的电化学生物传感器应进一步扩展用于检测广泛的分析物,并且在用于基因相关疾病的早期诊断的超灵敏生物传感平台的发展方面具有巨大的潜力。