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分子纳米剪切:一种利用交流感应纳米级流体流动剪切分子的创新方法。

Molecular nanoshearing: an innovative approach to shear off molecules with AC-induced nanoscopic fluid flow.

作者信息

Shiddiky Muhammad J A, Vaidyanathan Ramanathan, Rauf Sakandar, Tay Zhikai, Trau Matt

机构信息

Australian Institute for Bioengineering and Nanotechnology (AIBN), Corner College and Cooper Roads (Bldg 75), The University of Queensland, Brisbane QLD 4072, Australia.

1] Australian Institute for Bioengineering and Nanotechnology (AIBN), Corner College and Cooper Roads (Bldg 75), The University of Queensland, Brisbane QLD 4072, Australia [2] School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

Sci Rep. 2014 Jan 16;4:3716. doi: 10.1038/srep03716.

Abstract

Early diagnosis of disease requires highly specific measurement of molecular biomarkers from femto to pico-molar concentrations in complex biological (e.g., serum, blood, etc.) samples to provide clinically useful information. While reaching this detection limit is challenging in itself, these samples contain numerous other non-target molecules, most of which have a tendency to adhere to solid surfaces via nonspecific interactions. Herein, we present an entirely new methodology to physically displace nonspecifically bound molecules from solid surfaces by utilizing a newly discovered "tuneable force", induced by an applied alternating electric field, which occurs within few nanometers of an electrode surface. This methodology thus offers a unique ability to shear-off loosely bound molecules from the solid/liquid interface. Via this approach, we achieved a 5-fold reduction in nonspecific adsorption of non-target protein molecules and a 1000-fold enhancement for the specific capture of HER2 protein in human serum.

摘要

疾病的早期诊断需要在复杂的生物样本(如血清、血液等)中对飞摩尔至皮摩尔浓度的分子生物标志物进行高度特异性的测量,以提供临床有用信息。虽然达到这一检测限本身具有挑战性,但这些样本包含许多其他非目标分子,其中大多数倾向于通过非特异性相互作用附着在固体表面。在此,我们提出了一种全新的方法,通过利用由施加的交变电场诱导产生的新发现的“可调谐力”,从固体表面物理置换非特异性结合的分子,这种力出现在电极表面几纳米范围内。因此,这种方法具有独特的能力,能够从固/液界面剪切掉松散结合的分子。通过这种方法,我们实现了非目标蛋白质分子非特异性吸附减少5倍,以及人血清中HER2蛋白特异性捕获增强1000倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c851/3893656/94fe55f34e92/srep03716-f1.jpg

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