Ege University, Faculty of Pharmacy, Analytical Chemistry Department, Bornova, 35100 Izmir, Turkey.
Talanta. 2014 Jan;118:7-13. doi: 10.1016/j.talanta.2013.09.041. Epub 2013 Oct 7.
The multi-channel screen-printed array of electrodes (MUX-SPE16) was used in our study for the first time for electrochemical monitoring of nucleic acid hybridization related to different miRNA sequences (miRNA-16, miRNA-15a and miRNA-660, i.e, the biomarkers for Alzheimer disease). The MUX-SPE16 was also used for the first time herein for the label-free electrochemical detection of nucleic acid hybridization combined magnetic beads (MB) assay in comparison to the disposable pencil graphite electrode (PGE). Under the principle of the magnetic beads assay, the biotinylated inosine substituted DNA probe was firstly immobilized onto streptavidin coated MB, and then, the hybridization process between probe and its complementary miRNA sequence was performed at MB surface. The voltammetric transduction was performed using differential pulse voltammetry (DPV) technique in combination with the single-use graphite sensor technologies; PGE and MUX-SPE16 for miRNA detection by measuring the guanine oxidation signal without using any external indicator. The features of single-use sensor technologies, PGE and MUX-SPE16, were discussed concerning to their reproducibility, detection limit, and selectivity compared to the results in the earlier studies presenting the electrochemical miRNA detection related to different miRNA sequences.
我们首次在研究中使用多通道丝网印刷电极阵列 (MUX-SPE16) 用于电化学监测与不同 miRNA 序列(miRNA-16、miRNA-15a 和 miRNA-660,即阿尔茨海默病的生物标志物)相关的核酸杂交。MUX-SPE16 还首次用于本文中的无标记电化学检测核酸杂交结合磁珠 (MB) 测定,与一次性铅笔状石墨电极 (PGE) 相比。在磁珠测定的原理下,首先将生物素化的肌苷取代 DNA 探针固定在链霉亲和素涂覆的 MB 上,然后在 MB 表面进行探针与其互补 miRNA 序列之间的杂交过程。通过差分脉冲伏安法 (DPV) 技术与一次性石墨传感器技术相结合进行伏安转换;使用 PGE 和 MUX-SPE16 通过测量鸟嘌呤氧化信号来检测 miRNA,而无需使用任何外部指示剂。讨论了一次性传感器技术、PGE 和 MUX-SPE16 的特点,包括与早期研究中提出的与不同 miRNA 序列相关的电化学 miRNA 检测结果相比,其重现性、检测限和选择性。