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A Novel Approach to Produce Protein Nanopatterns by Combining Nanoimprint Lithography and Molecular Self-Assembly

机译:纳米压印光刻技术和分子自组装相结合产生蛋白质纳米图案的新方法

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We describe a novel parallel method for the patterning of proteins with nanoscale resolution.Combining nanoimprint lithography (NIL) and molecular assembly patterning by lift-off (MAPL),we produced streptavidin patterns with feature sizes in the order of 100 nm.A stamp is imprinted into a heated PMMA film followed by a dry etching step that converts the topography into a PMMA/Nb_2O_5 contrast.A biotin functionalized copolymer,poly(L-lysine)-graft-poly(ethylene glycol)-biotin (PLL-g-PEG/PEG-biotin),spontaneously adsorbs on the oxide surfaces.After PMMA lift-off,the background is backfilled with protein-resistant PLL-g-PEG.We show that streptavidin selectively adsorbs on the biotin areas and thus can be used as a universal platform for immobilization of biotin-tagged molecules.This novel process is a parallel patterning method that is fast,reproducible,and economic.The PEG-copolymer can be functionalized with a variety of bioactive groups and thus allows a great flexibility in terms of surface chemistry.
机译:我们描述了一种新颖的并行方法,用于以纳米级分辨率对蛋白质进行构图。结合纳米压印光刻(NIL)和通过剥离(MAPL)进行分子组装构图,我们制备了特征尺寸在100 nm左右的链霉亲和素构图。压印到加热的PMMA膜中,然后进行干蚀刻步骤,将形貌转换为PMMA / Nb_2O_5对比度。生物素官能化的共聚物,聚(L-赖氨酸)-接枝-聚(乙二醇)-生物素(PLL-g-PEG / PEG-生物素),自发地吸附在氧化物表面上.PMMA剥离后,背景被抗蛋白质的PLL-g-PEG填充。我们证明链霉亲和素选择性吸附在生物素区域,因此可以用作固定化生物素标记分子的通用平台。这种新颖的方法是一种并行,快速,可重复且经济的构图方法。PEG共聚物可通过多种生物活性基团进行功能​​化,因此在s方面具有极大的灵活性。表面化学。

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