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基于杂交作用的单个微球悬浮体对金纳米颗粒的声悬浮作用实现对 DNA 的皮摩尔生物传感的灵活选择性

Zeptomole Biosensing of DNA with Flexible Selectivity Based on Acoustic Levitation of a Single Microsphere Binding Gold Nanoparticles by Hybridization.

机构信息

Department of Chemistry , Tokyo Institute of Technology , Meguro-ku , Tokyo 152-8551 , Japan.

出版信息

ACS Sens. 2018 Sep 28;3(9):1870-1875. doi: 10.1021/acssensors.8b00748. Epub 2018 Sep 11.

Abstract

A novel scheme for DNA sensing at the zeptomole level is presented, based on the levitation of a single microsphere in a combined acoustic-gravitational (CAG) field. The levitation of a microsphere in the field is predominantly determined by its density. Capture and reporter probe DNAs are anchored on poly(methyl methacrylate) microsphere (PMMA) and gold nanoparticles (AuNPs), respectively, and a target DNA induces the binding of AuNPs on PMMA. This interparticle sandwich DNA-hybridization induces density increase in PMMA, which is detected as a shift in the levitation coordinate in the CAG field. The reporter DNAs are designed based on base-pair (bp) number selectivity, which is evaluated using direct interparticle hybridization between DNA-bound PMMA and complementary DNA-anchored AuNPs. Interestingly, the bp-number selectivity can be enlarged by lowering the reactant concentrations. Thus, the threshold bp, at which no density change is detected, can be adjusted by controlling the reactant concentrations. This strategy is extended to the sensing of HIV-2 DNA and single nucleotide polymorphism (SNP) detection of the KRAS gene by sandwich hybridization. In SNP detection, the present method selectively distinguishes wild-type DNA from mutant DNA differing by one nucleotide in the 21-nucleotide sequence by optimizing the lengths of probe DNAs and particle concentrations. This approach allows the detection of 1000 DNA molecules.

摘要

提出了一种基于单个微球在声重力(CAG)场中悬浮的新型纳升级 DNA 传感方案。微球在该场中的悬浮主要由其密度决定。捕获和报告探针 DNA 分别锚定在聚甲基丙烯酸甲酯(PMMA)微球和金纳米粒子(AuNPs)上,而目标 DNA 诱导 AuNPs 与 PMMA 结合。这种粒子间夹心 DNA 杂交导致 PMMA 密度增加,这可以在 CAG 场中悬浮坐标的变化中检测到。报告 DNA 是基于碱基对(bp)数量选择性设计的,这是通过 DNA 结合的 PMMA 与互补 DNA 锚定的 AuNPs 之间的直接粒子间杂交来评估的。有趣的是,通过降低反应物浓度可以放大 bp 数量选择性。因此,可以通过控制反应物浓度来调整检测不到密度变化的阈值 bp。该策略通过夹心杂交扩展到 HIV-2 DNA 的传感和 KRAS 基因的单核苷酸多态性(SNP)检测。在 SNP 检测中,通过优化探针 DNA 和粒子浓度的长度,本方法可以选择性地区分野生型 DNA 和突变型 DNA,突变型 DNA 在 21 个核苷酸序列中仅相差一个核苷酸。该方法允许检测 1000 个 DNA 分子。

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