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From Monochrome to Technicolor: Simple Generic Approaches to Multicomponent Protein Nanopatterning Using Siloxanes with Photoremovable Protein-Resistant Protecting Groups.

机译:从单色到彩色:使用具有光可移动蛋白质抗性保护基团的硅氧烷的多组分蛋白质纳米图案的简单通用方法。

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摘要

We show that sequential protein deposition is possible by photodeprotection of films formed from a tetraethylene-glycol functionalized nitrophenylethoxycarbonyl-protected aminopropyltriethoxysilane (NPEOC-APTES). Exposure to near-UV irradiation removes the protein-resistant protecting group, and allows protein adsorption onto the resulting aminated surface. The protein resistance was tested using proteins with fluorescent labels and microspectroscopy of two-component structures formed by micro- and nanopatterning and deposition of yellow and green fluorescent proteins (YFP/GFP). Nonspecific adsorption onto regions where the protecting group remained intact was negligible. Multiple component patterns were also formed by near-field methods. Because reading and writing can be decoupled in a near-field microscope, it is possible to carry out sequential patterning steps at a single location involving different proteins. Up to four different proteins were formed into geometric patterns using near-field lithography. Interferometric lithography facilitates the organization of proteins over square cm areas. Two-component patterns consisting of 150 nm streptavidin dots formed within an orthogonal grid of bars of GFP at a period of ca. 500 nm could just be resolved by fluorescence microscopy.
机译:我们表明,通过对由四乙二醇功能化的硝基苯基乙氧基羰基保护的氨基丙基三乙氧基硅烷(NPEOC-APTES)形成的膜进行光脱保护,可以实现顺序的蛋白质沉积。暴露于近紫外线下会除去抗蛋白质的保护基,并使蛋白质吸附到最终的胺化表面上。使用具有荧光标记的蛋白和通过黄色和绿色荧光蛋白(YFP / GFP)的微观和纳米构图以及沉积形成的两组分结构的显微光谱对蛋白的抗性进行了测试。在保护基保持完整的区域上的非特异性吸附可以忽略不计。还通过近场方法形成了多个成分图案。由于读写可以在近场显微镜中解耦,因此有可能在涉及不同蛋白质的单个位置执行顺序构图步骤。使用近场光刻技术,最多可以将四种不同的蛋白质形成几何图案。干涉光刻有助于在平方厘米区域上组织蛋白质。由150 nm链霉抗生物素蛋白点组成的两成分模式,在GFP的条形的正交网格中,形成的周期为大约。 500 nm可以通过荧光显微镜分辨。

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