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基于仿刺参状金纳米晶-多层层状石墨烯气凝胶和目标 DNA 诱导的循环式双扩增策略的人血液循环肿瘤 DNA 的高灵敏电化学检测

Highly sensitive electrochemical detection of circulating tumor DNA in human blood based on urchin-like gold nanocrystal-multiple graphene aerogel and target DNA-induced recycling double amplification strategy.

机构信息

The Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122, China.

School of Pharmaceutical Sciences, Jiangnan University, Wuxi, 214122, China.

出版信息

Anal Chim Acta. 2020 Jul 18;1121:17-25. doi: 10.1016/j.aca.2020.04.077. Epub 2020 May 5.

Abstract

Detection of circulating tumor DNA (ctDNA) is important approach to risk stratification and treatment response monitoring of cancer patients, but current method lacks of enough sensitivity and repeatability. The paper repors shape-controlled synthesis of gold nanocrystals via reduction of HAuCl with ascorbic acid. The synergy of CTAC, KBr, KI and L-glutathione creates urchin-like gold nanocrystals (U-Au) with more exposed high-index facets. Preparation of electrochemical sensing platform for ctDNA involves modification of U-Au-multiple graphene aerogel for target DNA-induced recycle amplification. DNA probe 1 (P1) with methylene blue (MB) hybridizes with DNA probe 2 with ferrocene (Fc) to form duplex DNA, which was attached to U-Au through Au-S bond. The ctDNA hybridizes with hairpin DNA 1 to open hairpin structure, triggering target DNA-induced recycle. Utilization of target DNA-induced recycling allows one target DNA to approach many MB probes to electrode surface and to leave many Fc probes from electrode surface, promoting significant signal amplification. The detection signal is enhanced by catalyzed redox of Fc and MB. Electrochemical response increases with ctDNA concentration from 0.1 to 1 × 10 fM with detection limit of 0.033 fM. The biosensor provides ultrahigh sensitivity, specificity and stability and was successfully applied in detection of ctDNA in human blood.

摘要

循环肿瘤 DNA(ctDNA)的检测是癌症患者风险分层和治疗反应监测的重要方法,但目前的方法缺乏足够的灵敏度和可重复性。本文报道了通过抗坏血酸还原 HAuCl 来合成具有规则形状的金纳米晶体。CTAC、KBr、KI 和 L-谷胱甘肽的协同作用,创造了具有更多暴露的高指数晶面的刺猬状金纳米晶体(U-Au)。用于 ctDNA 的电化学传感平台的制备涉及 U-Au-多石墨烯气凝胶的修饰,用于目标 DNA 诱导的循环放大。与亚甲基蓝(MB)杂交的 DNA 探针 1(P1)与具有二茂铁(Fc)的 DNA 探针 2 形成双链 DNA,该双链 DNA 通过 Au-S 键附着在 U-Au 上。ctDNA 与发夹 DNA 1 杂交以打开发夹结构,触发目标 DNA 诱导的循环。利用目标 DNA 诱导的循环可以使一个目标 DNA 接近许多 MB 探针到电极表面,并使许多 Fc 探针从电极表面离开,从而促进显著的信号放大。Fc 和 MB 的催化氧化还原作用增强了检测信号。电化学响应随 ctDNA 浓度从 0.1 到 1×10 fM 增加,检测限为 0.033 fM。该生物传感器具有超高的灵敏度、特异性和稳定性,并成功应用于人血中 ctDNA 的检测。

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