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通过粒子光刻技术制备蛋白质点阵阵列。

Fabrication of protein dot arrays via particle lithography.

作者信息

Taylor Zachary R, Patel Krupa, Spain Travis G, Keay Joel C, Jernigen Jeremy D, Sanchez Ernest S, Grady Brian P, Johnson Matthew B, Schmidtke David W

机构信息

University of Oklahoma Bioengineering Center, School of Chemical, Biological, and Materials Engineering, Homer L. Dodge Department of Physics and Astronomy, Norman, OK 73019, USA.

出版信息

Langmuir. 2009 Sep 15;25(18):10932-8. doi: 10.1021/la901512z.

Abstract

The ability to pattern a surface with proteins on both the nanometer and the micrometer scale has attracted considerable interest due to its applications in the fields of biomaterials, biosensors, and cell adhesion. Here, we describe a simple particle lithography technique to fabricate substrates with hexagonally patterned dots of protein surrounded by a protein-repellent layer of poly(ethylene glycol). Using this bottom-up approach, dot arrays of three different proteins (fibrinogen, P-selectin, and human serum albumin) were fabricated. The size of the protein dots (450 nm to 1.1 microm) was independent of the protein immobilized but could be varied by changing the size of the latex spheres (diameter=2-10 microm) utilized in assembling the lithographic bead monolayer. These results suggest that this technique can be extended to other biomolecules and will be useful in applications where arrays of protein dots are desired.

摘要

在纳米和微米尺度上对表面进行蛋白质图案化处理的能力,因其在生物材料、生物传感器和细胞黏附等领域的应用而备受关注。在此,我们描述了一种简单的粒子光刻技术,用于制造具有六边形图案化蛋白质点的基底,这些蛋白质点被聚乙二醇的蛋白质排斥层所包围。采用这种自下而上的方法,制备了三种不同蛋白质(纤维蛋白原、P-选择素和人血清白蛋白)的点阵。蛋白质点的尺寸(450纳米至1.1微米)与固定的蛋白质无关,但可以通过改变用于组装光刻珠单层的乳胶球(直径 = 2 - 10微米)的尺寸来改变。这些结果表明,该技术可以扩展到其他生物分子,并且在需要蛋白质点阵的应用中将会很有用。

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