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分子计数免费和电化学发光单分子免疫分析与双稳定剂帽 CdSe 纳米晶体作为标签。

Molecular-Counting-Free and Electrochemiluminescent Single-Molecule Immunoassay with Dual-Stabilizers-Capped CdSe Nanocrystals as Labels.

机构信息

School of Chemistry and Chemical Engineering, Shandong University , Jinan 250100, China.

Department of Chemistry and Biochemistry, The University of Southern Mississippi , Hattiesburg, Mississippi 39406, United States.

出版信息

Anal Chem. 2016 May 17;88(10):5482-8. doi: 10.1021/acs.analchem.6b00967. Epub 2016 May 3.

Abstract

Biorelated single-molecule detection (SMD) has been achieved typically by imaging the redox fluorescent labels and then determining each label one by one. Herein, we demonstrated that the capping agents (i.e., mercaptopropionic acid and sodium hexametaphosphate) can facilitate the electrochemical involved hole (or electron) injecting process and improve the stability of the dual-stabilizers-capped CdSe nanocrystals (NCs), so that the CdSe NCs could be electrochemically and repeatedly inspired to excited states by giving off electrochemiluminescence (ECL) in a cyclic pattern. With the CdSe NCs as ECL label and carcinoembryonic antigen (CEA) as target molecule, a convenient single-molecule immunoassay was proposed by simply detecting the ECL intensity of the dual-stabilizers-capped CdSe NCs in a sandwich-typed immune complex. The limit of detection is 0.10 fg/mL at S/N = 3, which corresponds to about 6-8 CEA molecules in 20 μL of serum sample. Importantly, the ECL spectra of both CdSe NCs and its conjugate with probe antigen in the immune complex were almost identical to the photoluminescence spectrum of bare CdSe NCs, indicating that all emissions were originated from the same excited species. The molecular-counting-free and ECL-based SMD might be a promising alternative to the fluorescent SMD.

摘要

生物相关的单分子检测(SMD)通常通过对氧化还原荧光标记物进行成像,然后逐个确定每个标记物来实现。在此,我们证明了封端剂(即巯基丙酸和六偏磷酸钠)可以促进电化学涉及的空穴(或电子)注入过程,并提高双稳定剂封端的 CdSe 纳米晶体(NCs)的稳定性,从而使 CdSe NCs 能够通过以循环模式发出电化学发光(ECL)而被电化学和重复激发到激发态。以 CdSe NCs 作为 ECL 标记物和癌胚抗原(CEA)作为靶分子,通过简单检测夹心型免疫复合物中双稳定剂封端的 CdSe NCs 的 ECL 强度,提出了一种方便的单分子免疫分析方法。检测限在 S/N = 3 时为 0.10 fg/mL,相当于 20 μL 血清样品中约 6-8 个 CEA 分子。重要的是,免疫复合物中 CdSe NCs 及其与探针抗原的共轭物的 ECL 光谱与裸 CdSe NCs 的光致发光光谱几乎相同,表明所有发射都来自相同的激发态。无分子计数和基于 ECL 的 SMD 可能是荧光 SMD 的一种有前途的替代方法。

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