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从黑白到彩色:使用具有光解蛋白质保护基团的硅氧烷实现多组分蛋白质纳米图案化的简单通用方法。

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

机构信息

Department of Chemistry, University of Sheffield , Brook Hill, Sheffield S3 7HF, United Kingdom.

Department of Physics and Astronomy, University of Sheffield , Sheffield S3 7RH, United Kingdom.

出版信息

Langmuir. 2017 Sep 5;33(35):8829-8837. doi: 10.1021/acs.langmuir.7b01255. Epub 2017 Jun 7.

DOI:10.1021/acs.langmuir.7b01255
PMID:28551995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5588097/
Abstract

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.

摘要

我们通过光解保护由四乙二醇功能化的硝基苯乙氧羰基保护的氨丙基三乙氧基硅烷(NPEOC-APTES)形成的薄膜,证明了顺序蛋白质沉积是可能的。近紫外线照射去除了蛋白质抗性保护基团,并允许蛋白质吸附到所得的氨基化表面上。通过使用带有荧光标记的蛋白质和通过微图案化和黄色和绿色荧光蛋白(YFP/GFP)的纳米图案化和沉积形成的两组件结构的微光谱,测试了蛋白质的抗性。非特异性吸附到保护基团保持完整的区域可以忽略不计。也可以通过近场方法形成多组分图案。由于近场显微镜中的读取和写入可以解耦,因此可以在单个位置进行涉及不同蛋白质的顺序图案化步骤。使用近场光刻术,多达四种不同的蛋白质被制成几何图案。干涉光刻术有利于在平方厘米区域上组织蛋白质。在约 500nm 的 GFP 棒正交网格内形成的由 150nm 链霉亲和素点组成的两组件图案,可以通过荧光显微镜刚刚分辨出来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/649ab5f21f83/la-2017-012554_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/1a52aab5606b/la-2017-012554_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/de1296b1cc5a/la-2017-012554_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/9b958807117b/la-2017-012554_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/45b31dd8c259/la-2017-012554_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/f6cbdbaa2d46/la-2017-012554_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/649ab5f21f83/la-2017-012554_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/1a52aab5606b/la-2017-012554_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/de1296b1cc5a/la-2017-012554_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/9b958807117b/la-2017-012554_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/45b31dd8c259/la-2017-012554_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/f6cbdbaa2d46/la-2017-012554_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caf1/5588097/649ab5f21f83/la-2017-012554_0006.jpg

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