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通过金纳米粒子引发的均相还原测定法进行亚皮摩尔 DNA 的可视化检测:迈向广义的灵敏度增强策略。

Visual detection of sub-femtomole DNA by a gold nanoparticle seeded homogeneous reduction assay: toward a generalized sensitivity-enhancing strategy.

机构信息

CAS Key Laboratory of Soft Matter Chemistry, Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Rd., Hefei, Anhui 230026, China.

出版信息

Biosens Bioelectron. 2010 Apr 15;25(8):1984-8. doi: 10.1016/j.bios.2010.01.012. Epub 2010 Jan 18.

Abstract

Gold nanoparticles (AuNPs) have been employed to design colorimetric visual sensing assays toward the detections of various targets including DNA, based on the aggregation induced color transitions of AuNPs. However, the relatively high detection limit (LOD 10nM) in the case of DNA detection has become a stumbling block on the road of the further development and applications of these assays. This research aims at overcoming this limit by virtue of a seeded gold reduction strategy. Typically, low concentrations of 13 nm AuNPs modified with suitable DNA probes are allowed to hybridize with a DNA target to form aggregates, which are then transferred into a gold-enhancing cocktail for further depositions of more gold on the initial AuNP seeds. The color of the assay thus sensitively reflects the initial aggregation status of the 13 nm AuNPs, which can be related to the concentrations of the DNA target. This assay has a sensitivity that is at least 25-50 times improved. Under still not fully optimized conditions, 0.4 fmol DNA in a 2 microL sample can be confidently detected with the ability of distinguishing a single base mutation. It does not require isolations of the 13 nm AuNP aggregates during analyses and shares the advantages of a homogeneous assay, including simplicity, adaptability, convenience, and being free of interferences due to non-specific surface adsorptions.

摘要

金纳米颗粒 (AuNPs) 已被用于设计比色视觉传感测定法,以检测各种目标物,包括 DNA,这是基于 AuNPs 的聚集诱导的颜色转变。然而,在 DNA 检测的情况下,相对较高的检测限(LOD 10nM)已成为这些测定法进一步发展和应用的绊脚石。本研究旨在通过种子金还原策略克服这一限制。通常,允许低浓度的 13nmAuNPs 与合适的 DNA 探针杂交形成聚集体,然后将其转移到金增强鸡尾酒中,以在初始 AuNP 种子上进一步沉积更多的金。测定法的颜色因此灵敏地反映了 13nmAuNPs 的初始聚集状态,这与 DNA 靶标浓度有关。该测定法的灵敏度提高了至少 25-50 倍。在尚未完全优化的条件下,可以自信地检测 2μL 样品中 0.4fmol 的 DNA,并且具有区分单个碱基突变的能力。它在分析过程中不需要分离 13nmAuNP 聚集体,并且具有均相测定法的优点,包括简单、适应性、方便,并且由于非特异性表面吸附而不受干扰。

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