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基于电致化学发光共振能量转移放大平台电化学合成银纳米簇用于载脂蛋白 A1 的检测。

Electrochemical synthesis of silver nanoclusters on electrochemiluminescent resonance energy transfer amplification platform for Apo-A1 detection.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Talanta. 2018 May 1;181:32-37. doi: 10.1016/j.talanta.2017.12.063. Epub 2017 Dec 22.

DOI:10.1016/j.talanta.2017.12.063
PMID:29426519
Abstract

Herein, a novel electrochemiluminescence resonance energy transfer (ERET) strategy between in situ electrogenerated silver nanoclusters (AgNCs) as the donor and Ru(bpy)(5-NH-1,10-phen)Cl (Ru(II)) as the acceptor was reported, which was applied for the construction of a ultrasensitive immunosensor for the determination of apolipoprotein-A1 (Apo-A1). Notably, the Ag NCs were in suit electro-reducted on glassy carbon electrode (GCE) based on a simple, fast and controllable electrochemical technique, which acted as not only biocompatible ECL emitters, but also protein immobilization platform via Ag-N or Ag-S bond. Subsequently, the acceptor probe was constructed by modifying Ru(II) and secondary antibody on the nanocarriers of carboxyl-functionalized MWCNTs. Based on the sandwiched immunoassay method, the ECL signals declining at 449nm (Ag NCs) and the increasing at 650nm (Ru(II)) both reflect the amount of Apo-A1. By measuring the ratio of ECL/ECL, we could accurately quantify the concentration of Apo-A1 in range from 1.0pg/mL to 1.0ng/mL and limit of detection down to 0.33pg/mL, which opened up a new research direction for ultrasensitive ECL bioanalysis based metal NCs.

摘要

本文报道了一种新的电化学发光共振能量转移(ERET)策略,即在体电生成的银纳米簇(AgNCs)作为供体,Ru(bpy)(5-NH-1,10-phen)Cl(Ru(II))作为受体。该策略被应用于构建一种用于测定载脂蛋白-A1(Apo-A1)的超灵敏免疫传感器。值得注意的是,Ag NCs 是基于一种简单、快速和可控的电化学技术在玻碳电极(GCE)上原位电还原的,它不仅可以作为生物相容性的 ECL 发射器,还可以通过 Ag-N 或 Ag-S 键作为蛋白质固定化平台。随后,将 Ru(II)和第二抗体修饰在羧基功能化 MWCNTs 的纳米载体上,构建了受体探针。基于三明治免疫测定法,在 449nm(Ag NCs)处的 ECL 信号衰减和在 650nm(Ru(II))处的 ECL 信号增强均反映了 Apo-A1 的含量。通过测量 ECL/ECL 的比值,我们可以在 1.0pg/mL 至 1.0ng/mL 的范围内准确地定量 Apo-A1 的浓度,检测限低至 0.33pg/mL,为基于金属 NCs 的超灵敏 ECL 生物分析开辟了新的研究方向。

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