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基于 DNA 的化学发光纳米探针用于高灵敏和选择性检测汞(II)离子。

DNA-based chemiluminescent nanoprobes for highly sensitive and selective detection of mercury(II) ion.

机构信息

Key Laboratory of Eco-chemical Engineering, Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.

出版信息

Luminescence. 2013 Nov-Dec;28(6):847-52. doi: 10.1002/bio.2444. Epub 2012 Oct 23.

Abstract

A simple and sensitive DNA-stablized gold nanoparticle (AuNP)-based chemiluminescent (CL) probe for detecting mercury ion (Hg(2+)) in aqueous solution has been developed. The CL strategy relies upon the catalytic activity of unmodified AuNPs on the luminol-H2 O2 CL reaction, and the interaction of unmodified AuNPs with DNA. The unmodified AuNPs can effectively differentiate unstructured and folded DNA. The DNA desorbs from AuNPs in the presence of Hg(2+), leading to the increase in CL signal. By rationally varying the number of thymine in single-strand oligonucleotides, the detection range could be tuned. Employing single-strand oligonucleotides with 14 thymine in the detecting system, a sensitive linear range for Hg(2+) ions from 5.0 × 10(-10) to 1.0 × 10(-7) mol/L and a detection limit of 2.1 × 10(-10) mol/L are obtained. Changing the number of thymine to 10 and 6, it leads to a narrow detection range but a high sensitivity. Besides, DNA-based CL nanoprobes exhibit a remarkable selectivity for Hg(2+) ions over a variety of competing metal ions.

摘要

一种简单灵敏的基于 DNA 稳定的金纳米粒子(AuNP)化学发光(CL)探针,用于检测水溶液中的汞离子(Hg(2+))。CL 策略依赖于未修饰的 AuNPs 在鲁米诺-H2O2 CL 反应中的催化活性,以及未修饰的 AuNPs 与 DNA 的相互作用。未修饰的 AuNPs 可以有效地区分非结构和折叠的 DNA。在 Hg(2+)存在下,DNA 从 AuNPs 上解吸,导致 CL 信号增加。通过合理改变单链寡核苷酸中的胸腺嘧啶数量,可以调整检测范围。在检测系统中使用带有 14 个胸腺嘧啶的单链寡核苷酸,可以获得从 5.0×10(-10)到 1.0×10(-7)mol/L 的 Hg(2+)离子的灵敏线性范围和 2.1×10(-10)mol/L 的检测限。将胸腺嘧啶的数量改为 10 和 6,会导致检测范围变窄但灵敏度提高。此外,基于 DNA 的 CL 纳米探针对 Hg(2+)离子具有显著的选择性,优于多种竞争金属离子。

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