分裂适体微阵列小分子SPR成像检测

Feriel Melaine , Yoann Roupioz , Arnaud Buhot
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引用次数: 3

摘要

小分子检测仍然是诊断的一个挑战。由于它们的尺寸,在寻找选择性和敏感的探针以及基于夹层和/或信号放大分析开发适当的检测格式方面出现困难。在这项研究中,我们结合了多种策略:a)使用适体探针,选择短的寡核苷酸链,以便对小分子靶标具有很强的选择性;b)对适体的分裂版本进行序列工程,用于三明治试验;c)使用金纳米颗粒(AuNPs)放大表面等离子体共振成像(SPRi)信号。结合这三种策略,可以获得最先进的腺苷靶标检测限(LOD = 50 nM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small Molecule SPR Imaging Detection from Split Aptamer Microarrays

The small molecules detection remains a challenge for diagnostics. Due to their size, difficulties arise in finding selective and sensitive probes as well as developing appropriate detection format based on sandwich and/or signal amplification assays. In this study, we combine multiple strategies: a) the use of aptamer probes, short oligonucleotides strands selected in order to present strong selectivity for the small molecule target, b) the sequence engineering of split versions of the aptamer for a sandwich assay and c) the amplification of Surface Plasmon Resonance imaging (SPRi) signal by the use of gold nanoparticles (AuNPs). Combining those three strategies lead to state-of-the-art limit of detection (LOD = 50 nM) for the adenosine target.

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