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基于金纳米棒偶联酶辅助靶标循环放大的超灵敏无标记 ATP 检测

Ultrasensitive and label-free detection of ATP by using gold nanorods coupled with enzyme assisted target recycling amplification.

机构信息

School of Life Science, Jiangsu Normal University, Xuzhou, 221116, China.

School of Life Science, Jiangsu Normal University, Xuzhou, 221116, China.

出版信息

Anal Chim Acta. 2020 Apr 1;1104:117-124. doi: 10.1016/j.aca.2019.12.073. Epub 2019 Dec 31.

Abstract

Abnormal concentration of adenosine triphosphate (ATP) is directly asscociate with several diseases. Thus, sensitive detection of ATP is essential to early diagnosis of disease. Herein, we described an ultrasensitive strategy for ATP detection by using positively charged gold nanorods ((+)AuNRs) as an efficient fluorescence quenching platform, coupled with exonuclease Ⅲ (Exo Ⅲ) assisted target recycling amplification. To construct the sensor, DNA template that contained ATP aptamer was used for the formation of Ag nanoclusters signal probe (DNA/AgNCs), the structure of it could change to duplex after the interaction of it with ATP. Such DNA template or duplex DNA product could electrostatically adsorb onto (+)AuNRs surface, resulting in the quenching of the fluorescence signal due to the vicinity of AgNCs to (+)AuNRs. With the addition of Exo Ⅲ, DNA duplex could be hydrolyzed and released from (+)AuNRs surface, leading to the recovery of a strong fluorescent signal, while ATP could be regenerated for next target recycling. Combing the good fluorescence quenching ability of (+)AuNRs and the Exo Ⅲ assisted signal amplification, a low detection limit of 26 pM was achieved for ATP detection. Notably, the proposed method can be successfully applied for detecting ATP in serum samples, indicating a potential application value in early cancer diagnosis.

摘要

异常浓度的三磷酸腺苷 (ATP) 与多种疾病直接相关。因此,对 ATP 的灵敏检测对于疾病的早期诊断至关重要。在此,我们描述了一种通过使用带正电荷的金纳米棒((+)AuNRs)作为高效荧光猝灭平台,结合外切酶 Ⅲ(Exo Ⅲ)辅助目标循环放大来检测 ATP 的超灵敏策略。为了构建传感器,使用包含 ATP 适体的 DNA 模板形成 Ag 纳米团簇信号探针(DNA/AgNCs),其结构在与 ATP 相互作用后可以变成双链。这种 DNA 模板或双链 DNA 产物可以通过静电吸附到(+)AuNRs 表面,由于 AgNCs 靠近(+)AuNRs,导致荧光信号猝灭。加入 Exo Ⅲ 后,DNA 双链可以被水解并从 (+)AuNRs 表面释放,导致强荧光信号恢复,而 ATP 可以被再生用于下一次目标循环。结合(+)AuNRs 的良好荧光猝灭能力和 Exo Ⅲ 辅助的信号放大,实现了对 ATP 的低检测限为 26 pM。值得注意的是,该方法可成功应用于血清样品中 ATP 的检测,表明其在癌症早期诊断中有潜在的应用价值。

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