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通过微小带电荷的固态纳米孔识别单核苷酸。

Identification of Single Nucleotides by a Tiny Charged Solid-State Nanopore.

出版信息

J Phys Chem B. 2018 Aug 16;122(32):7929-7935. doi: 10.1021/acs.jpcb.8b06056. Epub 2018 Aug 8.

Abstract

Discrimination of single nucleotides by a nanopore remains a challenge because of the minor difference among the four types of single nucleotides. Here, the blockade currents induced by the translocation of single nucleotides through a 1.8 nm diameter silicon nitride nanopore have been measured. It is found that the single nucleotides are driven through the nanopore by an electroosmotic flow instead of electrophoretic force when a bias voltage is applied. The blockade currents for the four types of single nucleotides are unique and differentiable, following the order of the nucleotide volume. Also, the dwell time for each single nucleotide can last for several hundred microseconds with the advantage of the electroosmotic flow, which is helpful for single nucleotide identification. The dwell-time distributions are found to obey the first-passage time distribution from the 1D Fokker-Planck equation, from which the velocity and diffusion constant of each nucleotide can be deduced. Interestingly, the larger nucleotide is found to translocate faster than the smaller one inside the nanopore because the larger nucleotide has a larger surface area, which may produce larger drag force induced by the electroosmotic flow, which is validated by molecular dynamics simulations.

摘要

由于四种单核苷酸之间的细微差异,单核苷酸的区分仍然是一个挑战。在此,我们测量了通过 1.8nm 直径的氮化硅纳米孔的单核苷酸迁移引起的阻断电流。结果发现,当施加偏压时,单核苷酸通过电渗流而不是电泳力驱动穿过纳米孔。四种单核苷酸的阻断电流是独特且可区分的,遵循核苷酸体积的顺序。此外,由于电渗流的优势,每个单核苷酸的停留时间可以持续数百微秒,这有助于单核苷酸的识别。停留时间分布符合一维福克-普朗克方程的首次通过时间分布,从中可以推导出每个核苷酸的速度和扩散常数。有趣的是,我们发现较大的核苷酸在纳米孔内的迁移速度比较小的核苷酸快,因为较大的核苷酸具有更大的表面积,这可能会产生由电渗流引起的更大的阻力,这通过分子动力学模拟得到了验证。

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