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Ultrasensitive electrochemiluminescence detection of thrombin based on aptamer and cystamine modified gold nanoparticle probe

机译:基于适体和胱胺修饰的纳米金探针的凝血酶超灵敏电化学发光检测

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摘要

Recently, our group showed that one can detect specific oligonucleotides at low femtomolar levels with the electrochemiluminescence (ECL) biobarcode approach based on tris-(2, 2'-bipyridyl) ruthenium (TBR)-labeled cysteamine. It would be a significant advance to use the cysteamine assisted ECL biobarcode assay to detect protein targets in addition to DNA targets. Taking advantage of sandwich binding of two affinity aptamers for increased specificity, TBR-cysteamine as biobarcode for signal amplification and magnetic beads based ECL technology for rapid detection, a promising assay for thrombin quantification is developed. The sandwich complex could be selectively captured by micromagnetic particles and then quantified by ECL signals. Current cysteamine-Gold nanoparticle (GNP) conjugates based ECL biobarcode assay is expected to become a powerful tool for protein analysis.
机译:最近,我们的小组表明,可以使用基于tris-(2,2'-联吡啶基)钌(TBR)标记的半胱胺的电化学发光(ECL)生物条形码方法检测低飞摩尔水平的特定寡核苷酸。使用半胱胺辅助的ECL生物条形码测定法来检测除DNA靶标之外的蛋白质靶标将是一项重大进步。利用两个亲和适体的三明治结合来提高特异性,TBR-半胱胺作为生物条形码用于信号放大,基于磁珠的ECL技术用于快速检测,因此开发了一种很有希望的凝血酶定量测定方法。三明治复合物可以被微磁性粒子选择性地捕获,然后通过ECL信号进行定量。当前基于半胱胺-金纳米颗粒(GNP)缀合物的ECL生物条形码测定有望成为蛋白质分析的强大工具。

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