Faculty of Pharmacy, Analytical Chemistry Department, Ege University, Bornova, Izmir, 35100, Turkey; Biotechnology Department, Graduate School of Natural and Applied Sciences, Ege University, Bornova, Izmir, 35100, Turkey.
Faculty of Pharmacy, Analytical Chemistry Department, Ege University, Bornova, Izmir, 35100, Turkey; Biotechnology Department, Graduate School of Natural and Applied Sciences, Ege University, Bornova, Izmir, 35100, Turkey.
Anal Chim Acta. 2019 Sep 13;1071:78-85. doi: 10.1016/j.aca.2019.04.036. Epub 2019 Apr 22.
The development of a low-cost and disposable biosensing technologies has received a great interest of healthcare for the sensitive and reliable detection of single nucleotide mutation related to single nucleotide polymorphisms (SNPs). In the present study, an impedimetric biosensing platform based on zip nucleic acids (ZNA) was developed for the sensitive detection of Factor V Leiden (FV Leiden) mutation. After optimization of experimental parameters, the sequence selective hybridization between ZNA probe and target related to FV Leiden mutation was evaluated via electrochemical impedance spectroscopy technique (EIS) by measuring changes at the charge transfer resistance, R Sensitive and selective impedimetric analysis was performed using carbon nanofiber (CNF) modified screen printed electrodes (SPE) and multi-channel screen printed array of electrodes (MULTIx8 CNF-SPE) resulting in a relatively shorter time in comparison to conventional methods. The selectivity of ZNA probe to mutation-free DNA sequences was also investigated. The applicability of single-use ZNA biosensor was also tested in synthetic PCR samples containing a single base mutation.
基于拉链核酸(ZNA)的阻抗生物传感平台用于灵敏检测因子 V 莱顿(FV Leiden)突变。通过电化学阻抗谱技术(EIS)测量电荷转移电阻的变化,优化实验参数后,评估了 ZNA 探针与与 FV Leiden 突变相关的目标物之间的序列选择性杂交。使用碳纳米纤维(CNF)修饰的丝网印刷电极(SPE)和多通道丝网印刷电极阵列(MULTIx8 CNF-SPE)进行灵敏和选择性的阻抗分析,与传统方法相比,所需时间相对较短。还研究了 ZNA 探针对无突变 DNA 序列的选择性。还测试了一次性 ZNA 生物传感器在含有单个碱基突变的合成 PCR 样品中的适用性。