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基于 DNA 四面体介导的超支化杂交链式反应的高灵敏比率检测 Pb 离子

Ultrasensitive ratiometric detection of Pb using DNA tetrahedron-mediated hyperbranched hybridization chain reaction.

机构信息

Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin, 300191, PR China; Key Laboratory for Environmental Factors Control of Agro-product quality Safety, Ministry of Agriculture and Rural Affairs, Tianjin, 300191, China.

College of Chemistry and Chemical Engineering, Jinan, 250000, PR China.

出版信息

Anal Chim Acta. 2021 Feb 22;1147:170-177. doi: 10.1016/j.aca.2020.12.050. Epub 2020 Dec 29.

Abstract

A fluorescent sensing strategy was developed for rapid, highly sensitive and specific detection of lead (II) ion (Pb) on the basis of Pb DNAzyme-controlled tetrahedral DNA nanostructure (TDN)-mediated hyper-branched hybridization chain reaction (hHCR). In this strategy, DNA hairpins used for HCR amplification are modified on the four vertexes of TDN, which are then used to perform rapid TDN-hHCR in the presence of an initiator strand, producing large-sized cross-linked reaction products and thus giving greatly improved fluorescence resonance energy transfer (FRET) signal output. Pb DNAzyme catalyzes the cleavage of the initiator strand, inhibiting the initiation of TDN-hHCR and giving decreased FRET signal. Synergetic signal amplification of Pb DNAzyme-catalyzed cleavage reaction and subsequent TDN-hHCR confers the sensing platform with ultrahigh sensitivity. As low as 0.25 pM Pb can be detected by using either signal "turn-on" or "turn-off" mode. The whole detection process can be finished within 20 min. Strong anti-interference capacity of FRET-based ratiometric detection and high specificity of Pb DNAzyme endow the sensing platform with great practical application potential, which was demonstrated by the accurate detection of Pb in real river water, fruit, vegetable and grain samples.

摘要

基于 Pb DNA zyme 控制的四面体型 DNA 纳米结构(TDN)介导的超支化杂交链式反应(hHCR),开发了一种用于快速、高灵敏和特异性检测 Pb(II)离子(Pb)的荧光传感策略。在该策略中,用于 HCR 扩增的 DNA 发夹修饰在 TDN 的四个顶点上,然后在引发链的存在下进行快速 TDN-hHCR,产生大尺寸交联的反应产物,从而大大提高了荧光共振能量转移(FRET)信号输出。Pb DNAzyme 催化引发链的切割,抑制 TDN-hHCR 的起始,从而降低 FRET 信号。Pb DNAzyme 催化的切割反应和随后的 TDN-hHCR 的协同信号放大赋予了传感平台超高的灵敏度。通过使用信号“开启”或“关闭”模式,可检测到低至 0.25 pM 的 Pb。整个检测过程可以在 20 分钟内完成。基于 FRET 的比率检测的强抗干扰能力和 Pb DNAzyme 的高特异性赋予了传感平台巨大的实际应用潜力,通过对实际河水、水果、蔬菜和谷物样品中 Pb 的准确检测得到了证明。

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