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首页> 外文期刊>Analytical chemistry >Lateral Flow Aptasensor for Small Molecule Targets Exploiting Adsorption and Desorption Interactions on Gold Nanoparticles
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Lateral Flow Aptasensor for Small Molecule Targets Exploiting Adsorption and Desorption Interactions on Gold Nanoparticles

机译:用于小分子的侧向流动适用靶靶向金纳米颗粒上的吸附和解吸相互作用

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摘要

A lateral flow assay (LFA) can provide a rapid and cost-effective means to detect targets in situ; however, existing LFA formats (predominantly sandwich assays) are not suitable for small molecule targets. We present a new LFA design that probes the dissociation of aptamers from the surface of gold nanoparticles upon recognition of small targets. The target-induced removal of aptamer molecules from the surface of the colored particles results in the particles being captured on a test line comprised of the protein bovine serum albumin immobilized on nitrocellulose. On the other hand, in the absence of target, aptamer coated particles are protected from capture on the test line and are instead captured at a control line comprised of the protein lysozyme. This protein is strongly positively charged under measurement conditions and therefore captures all gold nanoparticles regardless of the presence of aptamers. The effectiveness and operation mechanism of this simply fabricated sensor was demonstrated by using a previously reported 35-mer aptamer for a small molecule, 17 beta-estradiol. The sensor exhibited nanomolar level of detection, excellent selectivity against potential interfering molecules, and robust operation in natural river water samples. The simplicity and performance of the sensor platform renders it applicable to a wide range of other aptamers targeting small molecules, as we demonstrated with a novel bisphenol A aptamer. Additionally, we show that our LFA design is not confined to the specific proteins used as test and control lines, provided that their charge is appropriate to modulate the interaction with aptamer-coated or bare nanoparticles.
机译:横向流动测定(LFA)可以提供快速且经济有效的方法,以检测原位的目标;然而,现有的LFA格式(主要是夹层测定)不适合小分子靶标。我们提出了一种新的LFA设计,探测在识别小靶标时从金纳米粒子的表面探测适体的解离。来自着色颗粒表面的靶诱导的Aptamer分子结果导致颗粒在由固定在硝酸纤维素上固定的蛋白质牛血清白蛋白组成的测试线上。另一方面,在没有靶的情况下,保护Aptamer涂覆的颗粒免受测试线上的捕获,而是在由蛋白质溶菌酶组成的控制线上捕获。在测量条件下,该蛋白质强烈带电,因此无论适体是否存在,都捕获所有金纳米颗粒。通过使用先前报道的35-MEL适体的小分子,17β-雌二醇来证明这种简单制造的传感器的有效性和操作机制。该传感器显示出纳摩尔检测水平,对潜在干扰分子的优异选择性,以及天然河水样品中的鲁棒操作。传感器平台的简单性和性能使其适用于靶向小分子的各种其他适体,正如我们用新型双酚A适体所示。此外,我们表明我们的LFA设计并不局限于用作测试和控制线的特定蛋白质,只要它们的电荷适用于调节与适体涂覆或裸纳米颗粒的相互作用。

著录项

  • 来源
    《Analytical chemistry》 |2017年第14期|共9页
  • 作者单位

    King Abdulaziz City Sci &

    Technol Riyadh 12371 Saudi Arabia;

    Victoria Univ Wellington Sch Biol Sci Wellington 6012 New Zealand;

    Victoria Univ Wellington Sch Chem &

    Phys Sci Wellington 6012 New Zealand;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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