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Determining Protein Size Using an Electrochemically Machined Pore Gradient in Silicon

机译:使用电化学加工的硅孔梯度测定蛋白质大小

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摘要

Porous silicon film displaying a distribution of pore dimensions can be generated by electrochemically etching silicon in aqueous ethanolic HF using an asymmetric electrode configuration. The median pore size and breadth of the size-distribution in the film can be set by adjusting the HF concentration, current density, and position of the counter electrode relative to the silicon electrode. Films with pore sizes in the range of a few nanometers are used is size-exclusion matrices to perform an on-chip determination of macromolecule dimensions. The test molecule used in this study is bovine serum albumin (BSA). Optical reflectivity spectra of the thin porous Si films display distinctive shifts in the Fabry-Perot fringes in regions of the film where the pore dimensions are larger than a critical size, interpreted to be the characteristic dimensions of the protein. Gating of the protein in and out of the porous films is demonstrated by adjustment of the solution pH below and above the pI (isoelectric point) value, respectively.
机译:通过使用不对称电极配置在乙醇酸水性 HF 中电化学蚀刻硅,可以产生显示孔尺寸分布的多孔硅膜。通过调整 HF 浓度、电流密度和对电极相对于硅电极的位置,可以设置薄膜中尺寸分布的中值孔径和宽度。孔径在几纳米范围内的薄膜是尺寸排阻矩阵,用于在芯片上测定大分子尺寸。本研究中使用的测试分子是牛血清白蛋白 (BSA)。薄多孔硅薄膜的光学反射光谱在薄膜孔尺寸大于临界尺寸的区域显示出法布里-珀罗条纹的独特变化,被解释为蛋白质的特征尺寸。通过分别将溶液pH值调整到低于和高于pI(等电点)值来证明蛋白质进出多孔膜的门控。

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