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预制多孔硅光子晶体上的化学图案化:迈向在精确位置对蛋白酶活性进行多重检测† 可获取电子补充信息(ESI):扫描电子显微镜图像、X射线光电子能谱结果及更多光学反射率数据。见DOI: 10.1039/c4tb00281d 点击此处获取额外数据文件。

Chemical patterning on preformed porous silicon photonic crystals: towards multiplex detection of protease activity at precise positions†Electronic supplementary information (ESI) available: SEM images, XPS result and more optical reflectivity data. See DOI: 10.1039/c4tb00281dClick here for additional data file.

作者信息

Zhu Ying, Soeriyadi Alexander H, Parker Stephen G, Reece Peter J, Gooding J Justin

机构信息

School of Chemistry and the Australian Centre for NanoMedicine , University of New South Wales , Sydney 2052 , Australia . Email:

School of Physics , University of New South Wales , Sydney 2052 , Australia.

出版信息

J Mater Chem B. 2014 Jun 21;2(23):3582-3588. doi: 10.1039/c4tb00281d. Epub 2014 Apr 8.

Abstract

Porous silicon (PSi) rugate filters modified with alkyne-terminated monolayers were chemically patterned using a combination of photolithography of photoresist and click chemistry. Two chemical functionalities were obtained by conjugating, click reactions, ethylene glycol moieties containing two different terminal groups to discrete areas towards the exterior of a PSi rugate filter. The patterning of biological species to the functionalized surface was demonstrated through the conjugation of fluorescein isothiocyanate labelled bovine serum albumin (FITC-BSA). Fluorescence microscopy showed selective positioning of FITC-BSA at discretely functionalized areas. Meanwhile, the optical information from precisely defined positions on the patterned surface was monitored by optical reflectivity measurements. The optical measurements revealed successful step-wise chemical functionalization followed by immobilization of gelatin. Multiplex detection of protease activity from different array elements on the patterned surface was demonstrated by monitoring the blue shifts in the reflectivity spectra resulted from the digestion of gelatin by subtilisin. Precise information from both individual elements and average population was acquired. This technique is important for the development of PSi into a microarray platform for highly parallel biosensing applications, especially for cell-based assays.

摘要

用炔基封端的单层修饰的多孔硅(PSi)波纹滤光片通过光刻胶光刻和点击化学相结合的方法进行化学图案化。通过点击反应将含有两种不同端基的乙二醇部分共轭到PSi波纹滤光片外部的离散区域,从而获得了两种化学功能。通过异硫氰酸荧光素标记的牛血清白蛋白(FITC-BSA)的共轭,证明了生物物种在功能化表面上的图案化。荧光显微镜显示FITC-BSA在离散功能化区域的选择性定位。同时,通过光学反射率测量监测图案化表面上精确定义位置的光学信息。光学测量表明成功进行了逐步化学功能化,随后固定了明胶。通过监测枯草杆菌蛋白酶消化明胶导致的反射光谱蓝移,证明了对图案化表面上不同阵列元件的蛋白酶活性进行多重检测。获得了来自单个元件和总体群体的精确信息。该技术对于将PSi开发成用于高度并行生物传感应用的微阵列平台非常重要,特别是对于基于细胞的分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db1f/4047838/f16b9cb30d95/c4tb00281d-s1.jpg

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