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首页> 外文期刊>Analytical Letters >Novel Sensitive Fluorometric Determination of Exonuclease I Using Polydopamine Nanospheres
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Novel Sensitive Fluorometric Determination of Exonuclease I Using Polydopamine Nanospheres

机译:新型敏感荧光测定Exonuclease I使用聚二胺纳米球

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A novel fluorescence sensing platform based on polydopamine nanospheres and 6-carboxyfluorescein labeled single-stranded DNA has been developed for monitoring the concentration of exonuclease I. Due to the interaction between single-stranded DNA and polydopamine nanospheres, the single-stranded DNA may be adsorbed on the surface of polydopamine nanospheres. The fluorescence of 6-carboxyfluorescein was subsequently quenched by the polydopamine nanospheres through energy transfer or electron transfer. However, the 6-carboxyfluorescein-labeled single-stranded DNA was specifically degraded by exonuclease I, producing mono or oligonucleotide fragments, which were not adsorbed by the polydopamine nanospheres, and thus the fluorescence signal was retained. The retained fluorescence of the sensing platform was found to be linear with the concentration of exonuclease I in the range of 0.15-10UmL(-1) with a detection limit of 0.05UmL(-1). In addition, the sensing platform was highly selective toward exonuclease I. Benefiting from the high efficiency and the simple design process, satisfactory performance has been successfully demonstrated for the determination of exonuclease I in complex samples.
机译:基于聚二胺纳米球和6-羧基荧光素标记的单链DNA的新型荧光传感平台用于监测外切核酸酶I的浓度。由于单链DNA和聚二胺纳米球之间的相互作用,可以吸附单链DNA在聚二胺纳米球的表面上。随后通过聚二胺纳米球通过能量转移或电子转移淬灭6-羧基荧光蛋白的荧光。然而,6-羧基荧光素标记的单链DNA通过外切核酸酶I特异性降解,产生单核或寡核苷酸片段,其未被聚二胺纳米球吸附,因此保留荧光信号。发现感测平台的保留荧光是线性的,其浓度在0.15-10umL(-1)的范围内,检测限为0.05uml(-1)。此外,传感平台对Exonuclease I具有高度选择性,从高效率和简单的设计过程中受益,成功地证明了在复杂样品中的外切核酸酶I的测定表现出令人满意的性能。

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