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首页> 外文期刊>ACS nano >Single-Stranded DNA Translocation Recordings through Solid-State Nanopores on Glass Chips at 10 MHz Measurement Bandwidth
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Single-Stranded DNA Translocation Recordings through Solid-State Nanopores on Glass Chips at 10 MHz Measurement Bandwidth

机译:通过在10 MHz测量带宽的玻璃芯片上的固态纳米孔单链DNA易位记录

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摘要

Accurate and low-cost analysis of biomole-cules is important for many applications. This work seeks to further improve the measurement bandwidths achievable with solid-state nanopores, which have emerged as an important platform for this analysis. We report single-stranded DNA translocation recordings at a bandwidth of 10 MHz copolymers of 80 (C(20)A(20)C(20)A(20)), 90 (C(30)A(30)C(30)), and 200 (C(50)A(50)C(50)A(50)) nucleotides through Si nanopores with effective diameters of 1.4-2.1 nm and effective membrane thicknesses 0.5-8.9 nm. By optimizing glass chips with thin nanopores and by integrating them with custom-designed amplifiers based on complementary metal-oxide-semiconductor technology, this work demonstrates detection of translocation events as brief as 100 ns with a signal-to-noise ratio exceeding seven at a measurement bandwidth of 10 MHz. We also report data robustness and variability across 13 pores of similar size and thickness, yielding a current blockade between 30 and 60% with a mean ionic current blockade (Delta I) of , similar to 3-9 nA and a characteristic dwell time of similar to 2-21 ns per nucleotide. These measurements show that characteristic translocation rates are at least 10 times faster than previously recorded. We detect transient intraevent fluctuations, multiple current levels within translocation events, and variability of DNA translocation event signatures and durations.
机译:对许多应用的准确和低成本分析对于许多应用很重要。这项工作寻求进一步改善具有固态纳米孔可实现的测量带宽,该测量带宽作为该分析的重要平台。在80(C(20)(20)C(20)A(20)),90(C(30)A(30)C(30)的带宽下报告10MHz共聚物的带宽以10MHz共聚物的带宽报告单链DNA易位记录。(C(30)A(30)C(30) )和200(50)℃(50)C(50)A(50))核苷酸通过Si纳米孔,其有效直径为1.4-2.1nm,有效膜厚度为0.5-8.9nm。通过使用薄纳米孔的优化玻璃芯片,并通过基于互补金属 - 氧化物半导体技术将它们与定制设计的放大器集成,这项工作表明,作为100ns为100ns的易位事件的检测,信号 - 噪声比超过七个测量带宽10 MHz。我们还报告跨越相似尺寸和厚度的13个孔的数据鲁棒性和可变性,产生30%至60%的电流阻断,其平均离子电流阻滞(Delta I)类似,类似于3-9 na和相似的特征停留时间每个核苷酸到2-21 ns。这些测量表明,特征易位率比以前记录的速度快10倍。我们检测到瞬态内部波动,易位事件中的多个电流水平,以及DNA易位事件签名和持续时间的可变性。

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