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Nanohole Arrays of Mixed Designs and Microwriting for Simultaneous and Multiple Protein Binding Studies

机译:纳米孔阵列的混合设计和微写用于同时和多种蛋白质结合研究

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摘要

We demonstrate using nanohole arrays of mixed designs and a microwriting process based on dip-pen nanolithography to monitor multiple, different protein binding events simultaneously in real time based on the intensity of Extraordinary Optical Transmission of nanohole arrays. The microwriting process and small footprint of the individual nanohole arrays enabled us to observe different binding events located only 16μm apart, achieving high spatial resolution. We also present a novel concept that incorporates nanohole arrays of different designs to improve confidence and accuracy of binding studies. For proof of concept, two types of nanohole arrays, designed to exhibit opposite responses to protein bindings, were fabricated on one transducer. Initial studies indicate that the mixed designs could help to screen out artifacts such as protein intrinsic signals, providing improved accuracy of binding interpretation.
机译:我们演示了使用混合设计的纳米孔阵列和基于浸笔式纳米光刻的微写过程,以基于纳米孔阵列非凡的光学透射强度同时实时监测多个不同的蛋白质结合事件。单个纳米孔阵列的微写过程和较小的占用空间使我们能够观察到相距仅16μm的不同结合事件,从而实现了高空间分辨率。我们还提出了一个新颖的概念,该概念结合了不同设计的纳米孔阵列,以提高结合研究的可信度和准确性。为了进行概念验证,在一个换能器上制造了两种类型的纳米孔阵列,这些阵列设计成对蛋白质结合表现出相反的响应。初步研究表明,混合设计可以帮助筛选出伪影,例如蛋白质内在信号,从而提高结合解释的准确性。

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