Esfandyarpour Rahim, Yang Lu, Koochak Zahra, Harris James S, Davis Ronald W
Stanford Genome Technology Center, 3165 Porter Dr., Palo Alto, CA, 94304, USA.
Department of Bioengineering, Stanford University, Stanford, CA, USA.
Biomed Microdevices. 2016 Feb;18(1):7. doi: 10.1007/s10544-016-0032-8.
The improvements in our ability to sequence and genotype DNA have opened up numerous avenues in the understanding of human biology and medicine with various applications, especially in medical diagnostics. But the realization of a label free, real time, high-throughput and low cost biosensing platforms to detect molecular interactions with a high level of sensitivity has been yet stunted due to two factors: one, slow binding kinetics caused by the lack of probe molecules on the sensors and two, limited mass transport due to the planar structure (two-dimensional) of the current biosensors. Here we present a novel three-dimensional (3D), highly sensitive, real-time, inexpensive and label-free nanotip array as a rapid and direct platform to sequence-specific DNA screening. Our nanotip sensors are designed to have a nano sized thin film as their sensing area (~ 20 nm), sandwiched between two sensing electrodes. The tip is then conjugated to a DNA oligonucleotide complementary to the sequence of interest, which is electrochemically detected in real-time via impedance changes upon the formation of a double-stranded helix at the sensor interface. This 3D configuration is specifically designed to improve the biomolecular hit rate and the detection speed. We demonstrate that our nanotip array effectively detects oligonucleotides in a sequence-specific and highly sensitive manner, yielding concentration-dependent impedance change measurements with a target concentration as low as 10 pM and discrimination against even a single mismatch. Notably, our nanotip sensors achieve this accurate, sensitive detection without relying on signal indicators or enhancing molecules like fluorophores. It can also easily be scaled for highly multiplxed detection with up to 5000 sensors/square centimeter, and integrated into microfluidic devices. The versatile, rapid, and sensitive performance of the nanotip array makes it an excellent candidate for point-of-care diagnostics, and high-throughput DNA analysis applications.
我们对DNA进行测序和基因分型能力的提升,为理解人类生物学和医学开辟了众多途径,并具有各种应用,尤其是在医学诊断方面。但是,由于两个因素,实现无标记、实时、高通量和低成本的生物传感平台以高灵敏度检测分子相互作用的进展一直受到阻碍:其一,传感器上缺乏探针分子导致结合动力学缓慢;其二,当前生物传感器的平面结构(二维)导致传质受限。在此,我们展示了一种新型的三维(3D)、高灵敏度、实时、廉价且无标记的纳米尖端阵列,作为用于序列特异性DNA筛选的快速直接平台。我们的纳米尖端传感器设计为具有纳米尺寸的薄膜作为其传感区域(约20纳米),夹在两个传感电极之间。然后将尖端与与感兴趣序列互补的DNA寡核苷酸缀合,通过传感器界面形成双链螺旋时的阻抗变化实时电化学检测该寡核苷酸。这种3D配置经过专门设计,以提高生物分子命中率和检测速度。我们证明,我们的纳米尖端阵列以序列特异性和高灵敏度的方式有效检测寡核苷酸,产生与浓度相关的阻抗变化测量结果,目标浓度低至10 pM,甚至能够区分单个错配。值得注意的是,我们的纳米尖端传感器无需依赖信号指示剂或荧光团等增强分子即可实现这种准确、灵敏的检测。它还可以轻松扩展用于高达每平方厘米5000个传感器的高度多重检测,并集成到微流控设备中。纳米尖端阵列的多功能、快速和灵敏性能使其成为即时诊断和高通量DNA分析应用的极佳候选者。