首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >A peptide nucleic acid-regulated fluorescence resonance energy transfer DNA assay based on the use of carbon dots and gold nanoparticles
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A peptide nucleic acid-regulated fluorescence resonance energy transfer DNA assay based on the use of carbon dots and gold nanoparticles

机译:基于使用碳点和金纳米颗粒的肽核酸调节荧光共振能量转移DNA测定

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摘要

A convenient fluorometric method was developed for specific determination of DNA based on peptide nuclei acid (PNA)-regulated fluorescence resonance energy transfer (FRET) between carbon dots (CDs) and gold nanoparticles (AuNPs). In this system, CDs that display lake blue fluorescence with excitation/emission maxima at 345/445 nm were used as fluorometric reporter, while AuNPs were used as fluorescence nanoquencher. A neutral PNA probe, which is designed to recognize the target DNA, was used as a coagulant to control the dispersion and aggregation of AuNPs. Without DNA, PNA can induce immediate AuNP aggregation, thus leading to the recovery of the FRET-quenched fluorescence emission of CDs. However, the addition of the complementary target DNA can protect AuNPs from being aggregated due to the formation of DNA/PNA complexes, which subsequently produces a high fluorescence quenching efficiency of CDs by dispersed AuNPs. Under optimized conditions, quantitative evaluation of DNA was achieved in a linear range of 5-100 nM with a detection limit of 0.21 nM. This method exhibited an excellent specificity towards fully matched DNA. In addition, the application of this assay for sensitive determination of DNA in cell lysate demonstrates its potential for bioanalysis and biodetection.
机译:开发了一种方便的荧光法,用于基于肽核酸(PNA) - 在碳点(CDS)和金纳米粒子(AUNP)之间的肽核酸(PNA) - 调节荧光共振能量转移(FRET)的DNA的特异性测定。在该系统中,用作荧光报道器的荧光/发射最大值的CDS展示湖蓝色荧光,含荧光记录器,而AUNPS用作荧光纳米烧结器。设计用于识别靶DNA的中性PNA探针用作控制AUNP的分散剂和聚集的凝结剂。没有DNA,PNA可以诱导立即AUNP聚集,从而导致恢复CD的荧光淬火荧光发射。然而,添加互补靶DNA可以保护由于DNA / PNA复合物的形成而受到聚集的,这随后通过分散的AUNP产生CD的高荧光猝灭效率。在优化条件下,在5-100nm的线性范围内实现DNA的定量评估,检测限为0.21nm。该方法对完全匹配的DNA表现出优异的特异性。此外,该测定的应用对于细胞裂解物中DNA的敏感测定证明了其对生物分析和生物化的可能性。

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