University of Turku, Department of Future Technologies, 20500, Turku, Finland.
University of Turku, Department of Biotechnology, 20520, Turku, Finland.
Sci Rep. 2017 Nov 16;7(1):15734. doi: 10.1038/s41598-017-16028-7.
We demonstrate an electrochemical sensor for detection of unlabeled single-stranded DNA using peptide nucleic acid (PNA) probes coupled to the field-effect transistor (FET) gate. The label-free detection relies on the intrinsic charge of the DNA backbone. Similar detection schemes have mainly concentrated on sensitivity improvement with an emphasis on new sensor structures. Our approach focuses on using an extended-gate that separates the FET and the sensing electrode yielding a simple and mass fabricable device. We used PNA probes for efficient hybridization in low salt conditions that is required to avoid the counter ion screening. As a result, significant part of the target DNA lies within the screening length of the sensor. With this, we achieved a wash-free detection where typical gate potential shifts are more than 70 mV with 1 µM target DNA. We routinely obtained a real-time, label- and wash-free specific detection of target DNA in nanomolar concentration with low-cost electronics and the responses were achieved within minutes after introducing targets to the solution. Furthermore, the results suggest that the sensor performance is limited by specificity rather than by sensitivity and using low-cost electronics does not limit the sensor performance in the presented sensor configuration.
我们展示了一种使用肽核酸 (PNA) 探针与场效应晶体管 (FET) 栅极偶联的电化学传感器,用于检测未标记的单链 DNA。这种无标记检测依赖于 DNA 骨架的固有电荷。类似的检测方案主要集中在提高灵敏度上,并强调新的传感器结构。我们的方法侧重于使用扩展栅极将 FET 和传感电极分开,从而得到一个简单且易于大规模制造的器件。我们使用 PNA 探针在低盐条件下进行高效杂交,这是避免抗衡离子屏蔽所必需的。结果,目标 DNA 的很大一部分位于传感器的屏蔽长度内。通过这种方式,我们实现了免洗检测,其中典型的栅极电位变化超过 70 mV,目标 DNA 浓度为 1 μM。我们使用低成本电子设备,在纳摩尔浓度下实时、无标记且无需清洗即可对目标 DNA 进行常规特异性检测,并且在将目标引入溶液后几分钟内即可获得响应。此外,结果表明,传感器性能受到特异性的限制,而不是灵敏度的限制,并且在所示的传感器配置中,使用低成本电子设备不会限制传感器性能。