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Stable fabrication of a large nanopore by controlled dielectric breakdown in a high-pH solution for the detection of various-sized molecules

机译:通过在高pH溶液中进行可控的介电击穿来稳定制造大型纳米孔以检测各种大小的分子

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摘要

For nanopore sensing of various-sized molecules with high sensitivity, the size of the nanopore should be adjusted according to the size of each target molecule. For solid-state nanopores, a simple and inexpensive nanopore fabrication method utilizing dielectric breakdown of a membrane is widely used. This method is suitable for fabricating a small nanopore. However, it suffers two serious problems when attempting to fabricate a large nanopore: the generation of multiple nanopores and the non-opening failure of a nanopore. In this study, we found that nanopore fabrication by dielectric breakdown of a SiN membrane under high-pH conditions (pH ≥ 11.3) could overcome these two problems and enabled the formation of a single large nanopore up to 40 nm in diameter within one minute. Moreover, the ionic-current blockades derived from streptavidin-labelled and non-labelled DNA passing through the fabricated nanopore were clearly distinguished. The current blockades caused by streptavidin-labelled DNA could be identified even when its concentration is 1% of the total DNA.
机译:对于具有高灵敏度的各种大小的分子的纳米孔感测,应根据每个目标分子的大小调整纳米孔的大小。对于固态纳米孔,广泛使用利用膜的介电击穿的简单且廉价的纳米孔制造方法。该方法适合于制造小的纳米孔。然而,当试图制造大的纳米孔时,它遭受两个严重的问题:多个纳米孔的产生和纳米孔的非开放破坏。在这项研究中,我们发现通过在高pH条件(pH≥11.3)下将SiN膜介电击穿来制造纳米孔可以克服这两个问题,并在一分钟内形成直径最大为40 nm的单个大纳米孔。此外,清楚地区分了源自链霉亲和素标记的和未标记的DNA穿过制造的纳米孔的离子电流阻滞作用。即使由链霉亲和素标记的DNA引起的当前封锁也可以被识别,即使其浓度为总DNA的1%。

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