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Detection of Pb~(2+) Based on Label-free Fluorescence Probe

机译:基于无标记荧光探针检测PB〜(2+)

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摘要

A simple and sensitive detection method for lead ions was developed, based on the G-quadruplex and label-free fluorescence probe. A appropriate G-rich oligonucleotide folded into stable quadruplex structure when mixed with lead in an aqueous solution. Subsequently, single-stranded nucleic acid specific nuclease was added. An oligonucleotide in quadruplex structure is markedly resistant to nuclease digestion. However, G-rich oligonucleotide mixed with other common mono- or divalent ions was completely digested in 5 min under optimized experimental conditions because no quadruplex or less stable quadruplex was formed. Finally, a positively charged pyrene probe was mixed with oligonucleotide in lead. Electrostatic interactions between oligonucleotide (a polyanion) and the probe induced aggregation of the probe, which in turn induced strong pyrene excimer emission. The intensity of the induced excimer emission was directly proportional to the amount of lead added. The detection limit of our method was 500 nM.
机译:基于G-Quadreplex和无标记荧光探针,开发了一种简单敏感的铅离子检测方法。当在水溶液中与铅混合时,将适当的G-富含寡核苷酸折叠成稳定的四氢结构。随后,加入单链核酸特异性核酸酶。四逆转录结构中的寡核苷酸显着抵抗核酸酶消化。然而,在优化的实验条件下在5分钟内完全消化与其他常见的单核离子混合的G-富核苷酸在优化的实验条件下被完全消化,因为没有形成Quadflex或更少的稳定性QuadRuple。最后,将带正电荷的芘探针与寡核苷酸中的铅混合。寡核苷酸(多沉膜)之间的静电相互作用和探针诱导探针的聚集,其递转诱导强芘准分子发射。诱导的准分子发射的强度与加入的铅的量成正比。我们方法的检测限为500nm。

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