首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Patterning of proteins and cells on functionalized surfaces prepared by polyelectrolyte multilayers and micromolding in capillaries
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Patterning of proteins and cells on functionalized surfaces prepared by polyelectrolyte multilayers and micromolding in capillaries

机译:通过聚电解质多层膜和毛细管微模制备的功能化表面上的蛋白质和细胞图案

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摘要

A method for protein and cell patterning on polyclectrolyte-coated surfaces using simple micromolding in capillaries (MIMIC) is described. MIMIC produced two distinctive regions. One contained polyethylene glycol (PEG) microstructures fabricated using photopolymerization that provided physical, chemical, and biological barriers to the nonspecific binding of proteins, bacteria, and fibroblast cells. The second region was the polyelectrolyte (PEL) coated surface that promoted protein and cell immobilization. The difference in surface functionality between the PEL region and background PEG microstructures resulted in simple patterning of biomolecules. Fluorescein isothiocyanate-tagged bovine serum albumin, E. coli expressing green fluorescence protein (GFP), and fibroblast cells were successfully bound to the exposed PEL surfaces at micron scale. Compared with the simple adsorption of protein, fluorescence intensity was dramatically improved (by about six-fold) on the PEL-modified surfaces. Although animal cell patterning is prerequisite for adhesive protein layer to survive on desired area, the PEL surface without adhesive proteins provides affordable microenvironment for cells. The simple preparation of functionatized surface but universal platform can be applied to various biomolecules such as proteins, bacteria, and cells. (c) 2007 Elsevier B.V. All rights reserved.
机译:描述了一种使用毛细管中的简单微成型(MIMIC)在聚电解质涂层表面上进行蛋白质和细胞构图的方法。 MIMIC产生了两个独特的地区。一种包含使用光聚合反应制备的聚乙二醇(PEG)微结构,该结构为蛋白质,细菌和成纤维细胞的非特异性结合提供了物理,化学和生物屏障。第二个区域是聚电解质(PEL)涂层表面,可促进蛋白质和细胞固定化。 PEL区和背景PEG微结构之间的表面功能差异导致生物分子的简单图案化。异硫氰酸荧光素标记的牛血清白蛋白,表达绿色荧光蛋白(GFP)的大肠杆菌和成纤维细胞成功地以微米级结合到暴露的PEL表面。与简单的蛋白质吸附相比,在PEL修饰的表面上荧光强度得到了显着提高(大约六倍)。尽管动物细胞的图案化是粘附蛋白层在所需区域生存的前提,但不含粘附蛋白的PEL表面为细胞提供了可承受的微环境。功能化表面但通用平台的简单制备可以应用于各种生物分子,例如蛋白质,细菌和细胞。 (c)2007 Elsevier B.V.保留所有权利。

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