New probe immobilizations by lipoate-diethalonamines or ethylene-glycol molecules for capacitance DNA chip

S. Carrara, A. Cavallini, Y. Leblebici, G. De Micheli, V. Bhalla, F. Valle, B. Samorì, L. Benini, B. Riccò, Inger Vikholm-Lundin, T. Munter
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引用次数: 8

Abstract

Label-free DNA detection is of crucial role to when developing point-of-care biochips to be used in personalized therapy. Capacitance detection is a promising technology for label-free DNA detection. However, data published in literature often show evident time drift, large standard deviation, scattered data points, and poor reproducibility. To solve these problems, alkanethiol molecules such as mercapto-hexanol are usually considered as blocking agents. The aim of the present paper is to investigate new blocking agents to further improve DNA probe surfaces. Data from AFM, SPR, florescence microscopy, and capacitance measurements are used to demonstrate the new lipoates molecules. Moreover precursor layers obtained by using Ethylene-glycol alkanethiols offer further improvements in terms of diminished detection errors. Film structure is investigated at the nano-scale to justify the detection improvements in terms of probe surface quality. This study demonstrates the superiority of lipoate and Ethylene-glycol molecules as blocking candidates when immobilizing molecular probes onto spot surfaces in label-free DNA biochip.
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用脂酸-二乙胺或乙二醇分子固定化电容DNA芯片的新型探针
无标记DNA检测在开发用于个性化治疗的即时生物芯片时起着至关重要的作用。电容检测是一种很有前途的无标记DNA检测技术。然而,文献中发表的数据往往存在明显的时间漂移,标准差大,数据点分散,重现性差。为了解决这些问题,硫己醇等烷硫醇分子通常被认为是阻滞剂。本文的目的是研究新的阻断剂,以进一步改善DNA探针表面。来自AFM, SPR,荧光显微镜和电容测量的数据被用来证明新的脂酸盐分子。此外,使用乙二醇烷硫醇获得的前驱体层在减少检测误差方面提供了进一步的改进。在纳米尺度上研究了薄膜结构,以证明探头表面质量的检测改进。本研究表明,在无标记DNA生物芯片中,将分子探针固定在斑点表面时,脂酸盐和乙二醇分子作为阻断候选物具有优势。
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