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通过自组装 DNA 折纸模板定向吸附实现常规纳米级蛋白质图案。

Regular Nanoscale Protein Patterns via Directed Adsorption through Self-Assembled DNA Origami Masks.

机构信息

Technical and Macromolecular Chemistry, Paderborn University , Warburger Strasse 100, 33098 Paderborn, Germany.

Department of Genomics, Biotechnology Center, Technische Universität Dresden , Tatzberg 47-51, 01307 Dresden, Germany.

出版信息

ACS Appl Mater Interfaces. 2016 Nov 16;8(45):31239-31247. doi: 10.1021/acsami.6b10535. Epub 2016 Nov 1.

Abstract

DNA origami has become a widely used method for synthesizing well-defined nanostructures with promising applications in various areas of nanotechnology, biophysics, and medicine. Recently, the possibility to transfer the shape of single DNA origami nanostructures into different materials via molecular lithography approaches has received growing interest due to the great structural control provided by the DNA origami technique. Here, we use ordered monolayers of DNA origami nanostructures with internal cavities on mica surfaces as molecular lithography masks for the fabrication of regular protein patterns over large surface areas. Exposure of the masked sample surface to negatively charged proteins results in the directed adsorption of the proteins onto the exposed surface areas in the holes of the mask. By controlling the buffer and adsorption conditions, the protein coverage of the exposed areas can be varied from single proteins to densely packed monolayers. To demonstrate the versatility of this approach, regular nanopatterns of four different proteins are fabricated: the single-strand annealing proteins Redβ and Sak, the iron-storage protein ferritin, and the blood protein bovine serum albumin (BSA). We furthermore demonstrate the desorption of the DNA origami mask after directed protein adsorption, which may enable the fabrication of hierarchical patterns composed of different protein species. Because selectivity in adsorption is achieved by electrostatic interactions between the proteins and the exposed surface areas, this approach may enable also the large-scale patterning of other charged molecular species or even nanoparticles.

摘要

DNA 折纸已成为一种广泛应用的方法,用于合成具有广泛应用前景的纳米结构,这些纳米结构在纳米技术、生物物理学和医学等各个领域都有应用。最近,由于 DNA 折纸技术提供了出色的结构控制,通过分子光刻方法将单个 DNA 折纸纳米结构的形状转移到不同材料中的可能性引起了越来越多的关注。在这里,我们使用云母表面上带有内部空腔的 DNA 折纸纳米结构有序单层作为分子光刻掩模,用于在大面积上制造规则的蛋白质图案。将掩蔽的样品表面暴露于带负电荷的蛋白质中,导致蛋白质被定向吸附到掩模孔中的暴露表面区域。通过控制缓冲液和吸附条件,可以将暴露区域的蛋白质覆盖率从单个蛋白质变化到密集的单层。为了证明这种方法的多功能性,我们制造了四种不同蛋白质的规则纳米图案:单链退火蛋白 Redβ 和 Sak、铁储存蛋白铁蛋白和血液蛋白牛血清白蛋白 (BSA)。我们还证明了在定向蛋白质吸附后 DNA 折纸掩模的解吸,这可能使不同蛋白质种类组成的分级图案的制造成为可能。由于蛋白质与暴露表面之间的静电相互作用实现了吸附的选择性,因此这种方法还可能使其他带电分子种类甚至纳米颗粒的大规模图案化成为可能。

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