Department of Chemical and Biomolecular Engineering, The Hong Kong University of Science and Technology, Kowloon, Hong Kong.
Department of Chemical and Biomolecular Engineering, The Hong Kong University of Science and Technology, Kowloon, Hong Kong; Division of Biomedical Engineering, The Hong Kong University of Science and Technology, Kowloon, Hong Kong.
Biosens Bioelectron. 2012 May 15;35(1):230-234. doi: 10.1016/j.bios.2012.02.054. Epub 2012 Mar 5.
A highly sensitive electrochemical DNA sensor that requires no probe immobilization has been developed based on a target recycling mechanism utilizing a DNA polymerase with a strand displacement activity. The electrochemical detection is realized by taking advantage of the difference in diffusivity between a free ferrocene-labeled peptide nucleic acid (Fc-PNA) and a Fc-PNA hybridized with a complementary DNA, while the DNA polymerase-assisted target recycling leads to signal generation and amplification. The hybridization of the target DNA opens up a stem-loop template DNA with the Fc-PNA hybridized to its extruded 5' end and allows a DNA primer to anneal and be extended by the DNA polymerase, which results in sequential displacement of the target DNA and the Fc-PNA from the template DNA. The displaced target DNA will hybridize with another template DNA, triggering another round of primer extension and strand displacement. The released Fc-PNA, due to its neutral backbone, has much higher diffusivity towards a negatively charged electrode, compared to that when it is hybridized with a negatively charged DNA. Therefore, a significantly enhanced signal of Fc can be observed. The outstanding sensitivity and simplicity make this approach a promising candidate for next-generation electrochemical DNA sensing technologies.
基于利用具有链置换活性的 DNA 聚合酶的靶标循环利用机制,开发了一种无需探针固定的高灵敏电化学 DNA 传感器。通过利用游离的被钌(II)复合物标记的肽核酸(Fc-PNA)与互补 DNA 杂交的 Fc-PNA 在扩散率上的差异,实现了电化学检测,而 DNA 聚合酶辅助的靶标循环导致信号的产生和放大。靶标 DNA 的杂交打开了茎环模板 DNA,其中 Fc-PNA 杂交到其伸出的 5'端,并允许 DNA 引物与模板 DNA 退火和延伸,从而导致靶标 DNA 和 Fc-PNA 从模板 DNA 上的连续置换。被置换的靶标 DNA 将与另一个模板 DNA 杂交,引发另一个引物延伸和链置换循环。释放的 Fc-PNA 由于其中性骨架,与带负电荷的 DNA 杂交时,其向带负电荷的电极的扩散率要高得多。因此,可以观察到 Fc 的信号显著增强。这种方法具有出色的灵敏度和简单性,使其成为下一代电化学 DNA 传感技术的有前途的候选者。