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基于 DNA 酶的量子点组装放大标签的高灵敏度电子检测铅。

DNAzyme-based highly sensitive electronic detection of lead via quantum dot-assembled amplification labels.

机构信息

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Biosens Bioelectron. 2011 Oct 15;28(1):135-8. doi: 10.1016/j.bios.2011.07.009. Epub 2011 Jul 18.

Abstract

An electronic DNAzyme sensor for highly sensitive detection of Pb(2+) is demonstrated by coupling the significant signal enhancement of the layer-by-layer (LBL) assembled quantum dots (QDs) with Pb(2+) specific DNAzymes. The presence of Pb(2+) cleaves the DNAzymes and releases the biotin-modified fragments, which further hybridize with the complementary strands immobilized on the gold substrate. The streptavidin-coated, QD LBL assembled nanocomposites were captured on the gold substrate through biotin-streptavidin interactions. Subsequent electrochemical signals of the captured QDs upon acid dissolution provide quantitative information on the concentrations of Pb(2+) with a dynamic range from 1 to 1000 nM. Due to the dramatic signal amplification by the numerous QDs, subnanomolar level (0.6 nM) of Pb(2+) can be detected. The proposed sensor also shows good selectivity against other divalent metal ions and thus holds great potential for the construction of general DNAzyme-based sensing platform for the monitoring of other heavy metal ions.

摘要

通过将层层组装量子点 (QDs) 的显著信号增强与 Pb(2+) 特异性 DNA 酶偶联,展示了一种用于高灵敏度检测 Pb(2+) 的电子 DNA 酶传感器。存在的 Pb(2+) 会切割 DNA 酶并释放出生物素修饰的片段,这些片段进一步与固定在金基底上的互补链杂交。通过生物素-链霉亲和素相互作用,将涂覆有链霉亲和素的 QD 层层组装纳米复合材料捕获在金基底上。酸溶解后捕获的 QD 的电化学信号提供了 Pb(2+) 浓度的定量信息,其动态范围为 1 至 1000 nM。由于大量 QDs 的信号显著放大,可检测到亚纳摩尔级 (0.6 nM) 的 Pb(2+)。该传感器还对其他二价金属离子表现出良好的选择性,因此在构建用于监测其他重金属离子的通用基于 DNA 酶的传感平台方面具有很大的潜力。

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