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利用等离子纳米平台实现完美匹配与错配序列的高选择性、裸眼、痕量区分。

Highly Selective, Naked-Eye, and Trace Discrimination between Perfect-Match and Mismatch Sequences Using a Plasmonic Nanoplatform.

出版信息

Anal Chem. 2018 Jun 19;90(12):7371-7376. doi: 10.1021/acs.analchem.8b00756. Epub 2018 Jun 6.

Abstract

A plasmonic nanoplatform to perform an enzyme-free, naked-eye, and trace discrimination of single-base mutation from fully matched sequence is reported. The nanoplatform showed great potential to enhance catalytic hairpin assembly (CHA) amplification efficiency and biocatalytic activity of hemin/G-quadruplex (DNAzyme). When human immunodeficiency virus (HIV) DNA biomarker was used as the model analyst, a naked-eye detection with high selectivity and high sensitivity down to 10 M in whole serum was achieved by observing red-to-blue color change. Single-base mismatch and two-base mismatch were detected at the low concentrations of 10 and 10 M, respectively. The naked-eye detection based on the enzyme-free plasmonic nanoplatform is expected to have potential applications ranging from quick detection and early diagnostics to point-of-care research.

摘要

报道了一种等离子纳米平台,可在无需酶的情况下,通过肉眼观察,从完全匹配的序列中痕量区分单碱基突变。该纳米平台极大地提高了催化发夹组装(CHA)扩增效率和血红素/G-四链体(DNA 酶)的生物催化活性。当将人类免疫缺陷病毒(HIV)DNA 生物标志物用作模型分析物时,通过观察颜色从红色变为蓝色,可在全血清中实现高选择性和高灵敏度的肉眼检测,检测下限低至 10 M。单碱基错配和双碱基错配分别在 10 和 10 M 的低浓度下被检测到。基于无酶等离子纳米平台的肉眼检测有望在快速检测、早期诊断到即时护理研究等领域得到广泛应用。

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