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通过扫描探针光刻技术对聚乙二醇修饰的硅表面上图案化的生物分子进行原位观察。

In situ observation of biomolecules patterned on a PEG-modified Si surface by scanning probe lithography.

作者信息

Choi Inhee, Kang Sung Koo, Lee Jeongjin, Kim Younghun, Yi Jongheop

机构信息

School of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Biomaterials. 2006 Sep;27(26):4655-60. doi: 10.1016/j.biomaterials.2006.04.023. Epub 2006 May 15.

Abstract

A Si(100) wafer was modified with methoxy-poly(ethylene glycol) (M-PEG silane) via a self-assembly technique and nano-/micro-sized patterns were then fabricated by scanning probe lithography. The protrusive silicon dioxide pattern was more reactive compared to the non-patterned area, i.e. the PEG deposited area. To demonstrate the feasibility of the submicron patterning of protein based on the anodic oxidation of the Si surface by atomic force microscopy (AFM), streptavidin labelled with Au-colloidal particle and non-labelled streptavidin were site-selectively immobilized on the patterned areas. The streptavidin-patterned surface produced by these procedures can be utilized for the detection of biotinylated materials, such as an antibody and an antigen. A patterned silicon surface is the basis of biosensing devices, in which the patterned areas serve as sensing elements that directly interact with bioanalytes, while the background of the substrate remains passive to the deposition of analytes, thus resulting in a high signal-to-noise ratio.

摘要

通过自组装技术用甲氧基聚乙二醇(M-PEG硅烷)对硅(100)晶片进行改性,然后通过扫描探针光刻制造纳米/微米尺寸的图案。与未图案化区域(即聚乙二醇沉积区域)相比,突出的二氧化硅图案具有更高的反应活性。为了证明基于原子力显微镜(AFM)对硅表面进行阳极氧化的蛋白质亚微米图案化的可行性,将用金胶体颗粒标记的链霉亲和素和未标记的链霉亲和素选择性地固定在图案化区域上。通过这些程序产生的链霉亲和素图案化表面可用于检测生物素化材料,如抗体和抗原。图案化的硅表面是生物传感装置的基础,其中图案化区域用作直接与生物分析物相互作用的传感元件,而底物的背景对分析物的沉积保持被动,从而产生高信噪比。

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