Polymer Electronics Research Centre, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
Analyst. 2010 Mar;135(3):488-94. doi: 10.1039/b912797f. Epub 2010 Jan 15.
Detection of specific sequences of target DNA is of high importance in many fields, especially in medicinal diagnostics. DNA sensors should exhibit fast response to minute concentrations of the target sequence and have the ability to distinguish single-base mismatches from fully complementary target. This study focuses on the response of an electrochemical, CdTe nanoparticle-modified hairpin DNA sensor. The stem-loop structured probes and the blocking poly(ethylene glycol) (PEG) molecules were self-assembled on the gold electrode through S-Au bonding, to form a mixed monolayer employed as the sensing platform. Water-soluble CdTe nanoparticles were covalently attached to the hairpin probes (HPPs) and impedance spectroscopy was used for investigation of the electron transfer processes at a modified gold electrode before and after hybridization with the target DNA. The sensor showed reliable and sensitive detection of 4.7 fM of target. Although the selectivity of the sensor towards one-base mismatch targets needs to be improved, discrimination of non-complementary targets was achieved.
在许多领域,特别是在医学诊断中,检测目标 DNA 的特定序列具有重要意义。DNA 传感器应该对目标序列的微小浓度快速响应,并具有区分单碱基错配与完全互补目标的能力。本研究重点研究了一种电化学 CdTe 纳米粒子修饰发夹 DNA 传感器的响应。茎环结构的探针和阻塞聚(乙二醇)(PEG)分子通过 S-Au 键自组装在金电极上,形成用作传感平台的混合单层。水溶性 CdTe 纳米粒子被共价连接到发夹探针(HPPs)上,并且在与目标 DNA 杂交前后,使用阻抗谱研究了修饰金电极上的电子转移过程。该传感器可可靠且灵敏地检测到 4.7 fM 的目标。尽管该传感器对单碱基错配靶标具有选择性,但仍需要进一步提高,同时可以区分非互补靶标。