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通过盐梯度和电压对纳米孔壁的电荷密度和电荷极性进行调制。

Modulation of Charge Density and Charge Polarity of Nanopore Wall by Salt Gradient and Voltage.

机构信息

Department of Chemical Engineering , National Taiwan University , Taipei 10617 , Taiwan.

Department of Chemistry, Faculty of Engineering , Istanbul University - Cerrahpasa , Avcılar, 34320 Istanbul , Turkey.

出版信息

ACS Nano. 2019 Sep 24;13(9):9868-9879. doi: 10.1021/acsnano.9b01357. Epub 2019 Jul 31.

Abstract

Surface charge plays a very important role in biological processes including ionic and molecular transport across a cell membrane. Placement of charges and charge patterns on walls of polymer and solid-state nanopores allowed preparation of ion-selective systems as well as ionic diodes and transistors to be applied in building biological sensors and ionic circuits. In this article, we show that the surface charge of a 10 nm diameter silicon nitride nanopore placed in contact with a salt gradient is not a constant value, but rather it depends on applied voltage and magnitude of the salt gradient. We found that even when a nanopore was in contact with solutions of pH equivalent to the isoelectric point of the pore surface, the pore walls became charged with voltage-dependent charge density. Implications of the charge gating for detection of proteins passing through a nanopore were considered, as well. Experiments performed with single 30 nm long silicon nitride nanopores were described by continuum modeling, which took into account the surface reactions on the nanopore walls and local modulation of the solution pH in the pore and at the pore entrances. The results revealed that manipulation of surface charge can occur without changing pH of the background electrolyte, which is especially important for applications where maintaining pH at a constant and physiological level is necessary. The system presented also offers a possibility to modulate polarity and magnitude of surface charges in a two-electrode setup, which previously was accomplished in more complex multielectrode systems.

摘要

表面电荷在包括离子和分子跨细胞膜运输在内的许多生物过程中起着非常重要的作用。在聚合物和固态纳米孔的壁上放置电荷和电荷图案,允许制备离子选择性系统以及离子二极管和晶体管,以应用于构建生物传感器和离子电路。在本文中,我们表明,与盐梯度接触的直径为 10nm 的氮化硅纳米孔的表面电荷不是一个恒定值,而是取决于所施加的电压和盐梯度的大小。我们发现,即使纳米孔与 pH 值与孔表面等电点相等的溶液接触,孔壁也会因电压相关的电荷密度而带电。还考虑了电荷门控对检测通过纳米孔的蛋白质的影响。通过连续体建模描述了带有单个 30nm 长氮化硅纳米孔的实验,该模型考虑了纳米孔壁上的表面反应以及孔内和孔入口处溶液 pH 的局部调制。结果表明,在不改变背景电解质 pH 值的情况下可以进行表面电荷的操纵,这对于需要将 pH 值保持在恒定和生理水平的应用尤为重要。所提出的系统还提供了在双电极设置中调制表面电荷极性和大小的可能性,这在以前需要在更复杂的多电极系统中完成。

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