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基于两种不同来源的金纳米探针的核酸检测策略。

Nucleic acid detection strategy using gold nanoprobe of two diverse origin.

机构信息

Centre for Nanobiotechnology, VIT, Vellore - 632014, Tamil Nadu, India.

Vector Control Research Centre, Indian Council of Medical Research, Madurai - 625002, Tamil Nadu, India.

出版信息

IET Nanobiotechnol. 2019 Dec;13(9):928-932. doi: 10.1049/iet-nbt.2018.5332.

Abstract

In recent years, nanoparticles especially with gold and silver nanoparticles based point of care diagnostic methods is being developed for the lethal diseases like dengue. This study focused to work on the dengue virus detection in a simplest method using gold nanoparticles probe (AuNPs) with thiol tagged single strand DNA (ss-DNA). A sensitive, fluorescence-based detection strategy was designed to examine and quantified the hybridisation process and also elucidated the behaviour of AuNPs before and after interaction of biomolecule. The detection process was focused on aggregation of gold nanoprobe in the presence of complementary strand (target region). Hence the percentage of aggregation was measured and as a result, the limit of detection was found to be 10 dilutions. Current detection method was highly sensitive, easy to perform and the reaction timing is rapid between 5 and 10 min, and it can be observed through naked eye.

摘要

近年来,基于金纳米粒子和银纳米粒子的纳米粒子的即时诊断方法被开发出来,用于诊断登革热等致命疾病。本研究专注于使用巯基标记的单链 DNA(ss-DNA)的金纳米粒子探针(AuNPs)以最简单的方法检测登革热病毒。设计了一种灵敏的基于荧光的检测策略来检测和定量杂交过程,并阐明了生物分子相互作用前后 AuNPs 的行为。检测过程集中在金纳米探针在互补链(靶区域)存在下的聚集上。因此,测量了聚集的百分比,并且结果发现检测限为 10 倍稀释。目前的检测方法具有很高的灵敏度,易于操作,反应时间在 5 到 10 分钟之间,并且可以通过肉眼观察到。

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