首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Improving Pb~(2+) detection using DNAzyme-based fluorescence sensors by pairing fluorescence donors with gold nanoparticles
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Improving Pb~(2+) detection using DNAzyme-based fluorescence sensors by pairing fluorescence donors with gold nanoparticles

机译:通过将荧光供体与金纳米颗粒配对,使用基于DNAzyme的荧光传感器改善Pb〜(2+)检测

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For previously reported fluorescence Pb~(2+) sensors, DNAzymes have lead to a significant increase in Pb~(2+) detecting sensitivity and specificity. However, these sensors suffer from incomplete fluorescence quenching and require additional steps for annealing DNAzymes and substrates as well as for removing the uncoupled substrates. In this study, we successfully overcome these issues by immobilizing the substrate nucleic acids on gold nanoparticles through thiol linkages. The immobilization of the substrate molecules to the gold nanoparticles lead to almost-complete fluorescence quenching and fast Pb~(2+) detection, without altering the Pb~(2+) specificity of the DNAzymes. After optimizing the concentration of DNAzymes, reaction time and pH, we could detect Pb~(2+) as low as 5nM within 20min without the preliminary and the post treatments. Considering the multi-color-fluorescence quenching capability of gold nanoparticles and the to-be-developed functional nucleic acids for other metal ions, this study could extend the application of DNAzymes to the detection of multiple heavy metal ions.
机译:对于以前报道的荧光Pb〜(2+)传感器,DNA酶导致Pb〜(2+)检测灵敏度和特异性显着提高。然而,这些传感器遭受不完全的荧光猝灭,并且需要额外的步骤来使DNA酶和底物退火以及去除未偶联的底物。在这项研究中,我们通过硫醇键将底物核酸固定在金纳米颗粒上,从而成功克服了这些问题。将底物分子固定在金纳米颗粒上可导致几乎完全的荧光猝灭和快速的Pb〜(2+)检测,而不会改变DNAzyme的Pb〜(2+)特异性。优化DNA酶的浓度,反应时间和pH后,我们可以在20min内检测到低至5nM的Pb〜(2+),而无需进行前处理和后处理。考虑到金纳米粒子的多色荧光猝灭能力和其他金属离子的待开发功能性核酸,这项研究可以将DNA酶的应用扩展到多种重金属离子的检测中。

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