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多层血红素/G-四链体包裹的金纳米粒子作为标签,通过化学发光成像实现超灵敏多重免疫分析。

Multilayer hemin/G-quadruplex wrapped gold nanoparticles as tag for ultrasensitive multiplex immunoassay by chemiluminescence imaging.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, Department of Chemistry, Nanjing University, Nanjing 210093, PR China.

出版信息

Biosens Bioelectron. 2013 May 15;43:372-8. doi: 10.1016/j.bios.2012.12.051. Epub 2012 Dec 31.

DOI:10.1016/j.bios.2012.12.051
PMID:23356995
Abstract

A multilayer hemin/G-quadruplex DNAzyme wrapped gold nanoparticle (M-DNAzyme/AuNP) tag was designed for ultrasensitive chemiluminescence (CL) imaging. By combining with a disposable protein array, an ultrasensitive and high-throughput multiplex CL immunoassay method was proposed for simultaneous detection of four cancer biomarkers. The M-DNAzyme/AuNP tag was prepared by assembling high ratio of alkylthiol-capped signal DNA containing multiple G-quadruplex sequences to biotinylated DNA on AuNPs and then reacting with hemin to form multilayer hemin/G-quadruplex DNAzyme units. It could be bound to the biotinylated secondary antibody of sandwich immunocomplex by biotin-streptavidin conjugation to catalyze a CL reaction on a protein array, which produced strong CL emission. Under optimal conditions, the CL signals could be simultaneously collected by a charge-coupled device for ultrasensitive multiplex CL imaging of cancer biomarkers. Using α-fetoprotein, human chorionic gonadotrophin-β, carcinoma antigen 125, and carcinoembryonic antigen as model analytes, the proposed immunoassay method showed high sensitivities and wide linear ranges in a simple, cheap and high throughput way. The M-DNAzyme/AuNP as a universal signal tag as well as the protein chip could be suitable for mass production for economical, portable and multianalyte assay, showing a promising potential in application to clinic and other relative fields.

摘要

设计了一种多层血红素/G-四链体 DNA 酶包裹的金纳米粒子(M-DNAzyme/AuNP)标记物,用于超灵敏化学发光(CL)成像。通过与一次性蛋白质芯片结合,提出了一种超灵敏和高通量的多重 CL 免疫分析方法,用于同时检测四种癌症生物标志物。M-DNAzyme/AuNP 标记物通过组装高比例含多个 G-四链体序列的烷基硫醇封端信号 DNA 与 AuNPs 上的生物素化 DNA 结合,然后与血红素反应形成多层血红素/G-四链体 DNA 酶单元。它可以通过生物素-链霉亲和素缀合与夹心免疫复合物的生物素化二抗结合,从而在蛋白质芯片上催化 CL 反应,产生强烈的 CL 发射。在最佳条件下,CL 信号可以通过电荷耦合器件同时收集,用于超灵敏的癌症生物标志物多重 CL 成像。使用α-胎蛋白、人绒毛膜促性腺激素-β、癌抗原 125 和癌胚抗原作为模型分析物,该免疫分析方法以简单、廉价和高通量的方式显示出高灵敏度和宽线性范围。M-DNAzyme/AuNP 作为通用信号标记物以及蛋白质芯片可适用于大规模生产,用于经济、便携和多分析物检测,在临床和其他相关领域具有广阔的应用前景。

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