A DNA-stabilized silver nanoclusters/graphene oxide-based platform for the sensitive detection of DNA through hybridization chain reaction

纳米团簇 石墨烯 荧光 连锁反应 检出限 DNA 杂交探针 猝灭(荧光) 材料科学 化学 氧化物 纳米技术 光化学 色谱法 生物化学 有机化学 物理 量子力学
作者
Siqi Zhang,Kun Wang,Kai-Bin Li,Wei Shi,Wen‐Ping Jia,Xiaoying Chen,Ting Sun,Deman Han
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:91: 374-379 被引量:111
标识
DOI:10.1016/j.bios.2016.12.060
摘要

A silver nanoclusters (AgNCs)/graphene oxide (GO)-based fluorescence sensor was developed for label-free DNA detection through hybridization chain reaction (HCR). A DNA sequence associated with the human immunodeficiency virus (HIV) was selected as a model target. Two DNA probes, hairpin probe 1 (H1) and hairpin probe 2 (H2), were partially complementary. GO was used as an adsorption material to capture the hairpin probes and a selective fluorescence quencher was used to reduce the background signal. Upon addition of AgNO3 and NaBH4, the AgNCs were synthesized at the terminals of the H1 and H2 probes. In the absence of target DNA (THIV), hybridization chain reaction (HCR) could not be triggered due to the stability of H1 and H2 probes. The hairpin probe-protected AgNCs attached to the GO surface, efficiently quenching fluorescence of the AgNCs. Therefore, the system showed very low background. In presence of THIV, the target triggered the chain-like assembly of H1 and H2 through HCR, generating a long chain of H1 and H2 complexes. The HCR product (AgNCs nanowires) could not be adsorbed on the surface of GO; hence, it generated a strong fluorescent signal based on the concentration of the target. Under the optimized conditions, the detection limit of the fluorescence sensor was 1.18nM, and hence it can be applied to clinical samples.

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