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Direct patterning of nanoparticles and biomolecules by liquid nanodispensing

机译:纳米粒子的直接模式生物分子由液体nanodispensing

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We report on the localized deposition of nanoparticles and proteins, nano-objects commonly used in many nanodevices, by the liquid nanodispensing (NADIS) technique which consists in depositing droplets of a solution through a nanochannel drilled at the apex of an AFM tip. We demonstrate that the size of spots can be adjusted from microns down to sub-50 nm by tuning the channel diameter, independently of the chemical nature of the solute. In the case of nanoparticles, we demonstrated the ultimate limit of the method and showed that large arrays of single (or pairs of) nanoparticles can be reproducibly deposited. We further explored the possibility to deposit different visible fluorescent proteins using NADIS without loss of protein function. The intrinsic fluorescence of these proteins is characteristic of their structural integrity; the retention of fluorescence after NADIS deposition demonstrates that the proteins are intact and functional. This study demonstrates that NADIS can be a viable alternative to other scanning probe lithography techniques since it combines high resolution direct writing of nanoparticles or biomolecules with the versatility of liquid lithography techniques.
机译:我们报告的局部沉积纳米颗粒和蛋白质,一般nano-objects在许多nanodevices,使用液体它由nanodispensing(气脉)技术通过沉淀液滴的一个解决方案在顶端的AFM纳米通道钻小费。证明斑点的大小这从微米到纳米的优化调整通道直径、独立的溶质的化学性质。纳米粒子,我们证明了极限的方法和显示大数组的单(双)纳米颗粒可再生产地沉积。矿床的可能性明显不同荧光蛋白使用气脉没有损失蛋白质的功能。这些蛋白质是他们的特征结构完整性;荧光气脉沉积后显示蛋白质是完整和功能。研究表明,气脉是可行的选择扫描探针光刻技术,因为它结合了高分辨率直接写纳米粒子和生物分子的多功能性液体光刻技术。

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