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DNA-Programmed plasmonic ELISA for the ultrasensitive detection of protein biomarkers

机译:用于超细蛋白质生物标志物的超细敏感检测的DNA编程等离子体酶

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摘要

We report a novel DNA-programmed plasmonic enzyme-linked immunosorbent assay (ELISA) for the ultrasensitive detection of protein biomarkers with the naked eye. The DNA-programmed plasmonic assay was based on two enzyme-free and isothermal nucleic acid amplification methods: hybridization chain reaction (HCR) and catalyzed hairpin assembly (CHA). In this study, a biotin-labeled DNA probe was utilized insteand of an enzyme-label probe in well-developed ELISA method. The biotin-labeled DNA probe was able to trigger the HCR and CHA processes, and the products could hybridize with DNAmodified gold nanoparticles (AuNPs) to induce the aggregation of the AuNPs and a color change in the solution. The developed method was able to detect as low as 1 pg mL~(-1) PSA target with the naked eye. Clinical serum samples demonstrated satisfactory results, indicating that the method is useful for early diagnostics and monitoring curative effects after a medical treatment. The developed method presents a simple and portable platform for ultrasensitive protein detection and has potential for point-of-care (POC) diagnostics in less developed areas.
机译:我们报告了一种新型DNA编程的等离子体酶联免疫吸附测定(ELISA),用于用肉眼进行蛋白质生物标志物的超细敏感检测。 DNA编程的等离子体测定基于两种无酶和等温核酸扩增方法:杂交链反应(HCR)和催化的发夹组装(CHA)。在该研究中,利用了一种生物素标记的DNA探针在发达的ELISA方法中insteand酶标签探针。生物素标记的DNA探针能够触发HCR和CHA方法,并且产品可以与DNamodified金纳米颗粒(AUNP)杂交,以诱导αUNP的聚集和溶液中的颜色变化。开发方法能够用肉眼检测低至1pg ml〜(-1)PSA靶标。临床血清样品展示了令人满意的结果,表明该方法可用于治疗后的早期诊断和监测治疗效果。开发方法提出了一种简单便携的用于超敏蛋白质检测的平台,并且在较少发达地区的护理点(POC)诊断具有潜力。

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