Niedzwiecki David J, Chou Yung-Chien, Xia Zehui, Thei Federico, Drndić Marija
Goeppert LLC, Pennovation Works, 3401 Grays Ferry Avenue, Philadelphia, Pennsylvania 19146, USA.
Department of Physics and Astronomy, David Rittenhouse Laboratory, University of Pennsylvania, 209 S. 33rd Street, Philadelphia, Pennsylvania 19103, USA.
Rev Sci Instrum. 2020 Mar 1;91(3):031301. doi: 10.1063/1.5138210.
Nanopore sensing is a powerful tool for the detection of biomolecules. Solid-state nanopores act as single-molecule sensors that can function in harsh conditions. Their resilient nature makes them attractive candidates for taking this technology into the field to measure environmental samples for life detection in space and water quality monitoring. Here, we discuss the fabrication of silicon nitride pores from ∼1.6 to 20 nm in diameter in 20-nm-thick silicon nitride membranes suspended on glass chips and their performance. We detect pure laboratory samples containing a single analyte including DNA, BSA, microRNA, TAT, and poly-D-lys-hydrobromide. We also measured an environmental (mixed-analyte) sample, containing Antarctic dirt provided by NASA Ames. For DNA measurements, in addition to using KCl and NaCl solutions, we used the artificial (synthetic) seawater, which is a mixture of different salts mimicking the composition of natural seawater. These samples were spiked with double-stranded DNA (dsDNA) fragments at different concentrations to establish the limits of nanopore sensitivity in candidate environment conditions. Nanopore chips were cleaned and reused for successive measurements. A stand-alone, 1-MHz-bandwidth Chimera amplifier was used to determine the DNA concentration in artificial seawater that we can detect in a practical time scale of a few minutes. We also designed and developed a new compact nanopore reader, a portable read-out device with miniaturized fluidic cells, which can obtain translocation data at bandwidths up to 100 kHz. Using this new instrument, we record translocations of 400 bp, 1000 bp, and 15000 bp dsDNA fragments and show discrimination by analysis of current amplitude and event duration histograms.
纳米孔传感是检测生物分子的强大工具。固态纳米孔可作为单分子传感器,能在恶劣条件下发挥作用。其坚韧的特性使其成为将该技术应用于实地测量环境样本以进行太空生命探测和水质监测的有吸引力的候选者。在此,我们讨论了在悬浮于玻璃芯片上的20纳米厚氮化硅膜中制造直径约为1.6至20纳米的氮化硅孔及其性能。我们检测了包含单一分析物的纯实验室样本,这些分析物包括DNA、牛血清白蛋白(BSA)、微小RNA、穿膜肽(TAT)和聚-D-赖氨酸氢溴酸盐。我们还测量了一个环境(混合分析物)样本,其中包含美国国家航空航天局艾姆斯研究中心提供的南极污垢。对于DNA测量,除了使用氯化钾(KCl)和氯化钠(NaCl)溶液外,我们还使用了人工(合成)海水,它是模拟天然海水成分的不同盐类的混合物。这些样本中加入了不同浓度的双链DNA(dsDNA)片段,以确定在候选环境条件下纳米孔灵敏度的极限。纳米孔芯片经过清洗后可重复用于后续测量。使用一台独立的1兆赫兹带宽的嵌合体放大器来确定我们能够在几分钟的实际时间尺度内检测到的人工海水中的DNA浓度。我们还设计并开发了一种新型紧凑型纳米孔读取器,这是一种带有小型化流体池的便携式读出设备,它能够在高达100千赫兹的带宽下获取转位数据。使用这种新仪器,我们记录了400碱基对、1000碱基对和15000碱基对dsDNA片段的转位情况,并通过分析电流幅度和事件持续时间直方图来进行区分。