首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Paper-based electrochemiluminescence determination of streptavidin using reticular DNA-functionalized PtCu nanoframes and analyte-triggered DNA walker
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Paper-based electrochemiluminescence determination of streptavidin using reticular DNA-functionalized PtCu nanoframes and analyte-triggered DNA walker

机译:使用网状DNA官能化PTCU纳米rames和分析物触发DNA步行者使用纸纸电化学素测定链霉抗生物素蛋白的测定

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摘要

A paper-based electrochemiluminescence (ECL) biosensor characterized by the signal amplification of reticular DNA-functionalized PtCu nanoframes (DNA-PtCuTNFs) and analyte-triggered DNA walker was developed for sensitive streptavidin assay. Silver microflower functionalized paper-based sensing platform was prepared to fix the hairpin strand (S1). With addition of the streptavidin, plenty of DNA walkers consisting of the walking strands (S2) labeled with biotin and streptavidin were established, which protected S2 from digestion via the terminal protection mechanism. The sequential introduction of the DNA walker and capture probe initiated the hairpin structure opening of S1 and strand displacement reaction (SDR) happening, causing the S2 release. Subsequently, S1 hybridized with S3. The free S2 further hybridized with adjacent S1 to trigger the next cycle. After multiple cycles, the DNA-PtCuTNFs, the fire-new signal enhancer, with remarkable peroxidase activity, were successfully attached onto the paper electrode via metal-catalyst-free click chemistry. Based on the SDR of the DNA walker and the catalysis of DNA-PtCuTNFs, a significantly boosted ECL signal of luminol was obtained. Under the optimal conditions, the developed sensor for streptavidin assay exhibited a low detection limit of 33.4 fM with a linear range from 0.1 pM to 0.1 mu M.
机译:为敏感的链霉抗生物素蛋白测定,开发了一种基于纸的电化学荧光(ECL)生物传感器,其特征在于网状DNA官能化PTCU纳米rames(DNA-PTCUTNFS)和分析物触发的DNA步行者。制备银微辊官能化的基于纸张的传感平台以固定发夹链(S1)。加入链霉抗生物素蛋白,建立了由与生物素和链霉抗生物素蛋白标记的步行股(S2)组成的大量DNA步行者,其通过端子保护机构免受消化的保护。 DNA步行者和捕获探针的顺序引入引发了S1的发夹结构开口和束置换反应(SDR),导致S2释放。随后,S1与S3杂交。使用相邻的S1进一步杂交的自由S2以触发下一个循环。经过多次循环,DNA-PTCUTNFS,火新信号增强剂具有显着的过氧化物酶活性,通过金属催化剂的咔哒化学成功地连接到纸电极上。基于DNA步行者的SDR和DNA-PTCUTNF的催化,获得了鲁米诺的显着提高ECL信号。在最佳条件下,用于链霉抗生物素蛋白测定的发达的传感器显示出33.4 fm的低检测限,线性范围为0.1μm至0.1μm。

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