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本文引用的文献

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Temperature dependence of electrochemical DNA charge transport: influence of a mismatch.电化学 DNA 电荷输运的温度依赖性:错配的影响。
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Electrochemical detection of point mutation based on surface hybridization assay conjugated allele-specific polymerase chain reaction.基于杂交反应偶联等位基因特异性聚合酶链反应的电化学检测点突变。
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Polarity-switching electrochemical sensor for specific detection of single-nucleotide mismatches.用于特异性检测单核苷酸错配的极性转换电化学传感器。
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Electrochemical detection of DNA mutations on a PNA-modified electrode utilizing a single-stranded DNA specific endonuclease.在经肽核酸修饰的电极上利用单链 DNA 特异性内切酶电化学检测 DNA 突变。
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利用微流控电化学DNA熔解曲线对单核苷酸多态性进行准确的合子特异性鉴别。

Accurate zygote-specific discrimination of single-nucleotide polymorphisms using microfluidic electrochemical DNA melting curves.

作者信息

Yang Allen H J, Hsieh Kuangwen, Patterson Adriana S, Ferguson B Scott, Eisenstein Michael, Plaxco Kevin W, Soh H Tom

机构信息

Department of Mechanical Engineering, University of California Santa Barbara (USA).

出版信息

Angew Chem Int Ed Engl. 2014 Mar 17;53(12):3163-7. doi: 10.1002/anie.201310059. Epub 2014 Feb 12.

DOI:10.1002/anie.201310059
PMID:24520069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3992926/
Abstract

We report the first electrochemical system for the detection of single-nucleotide polymorphisms (SNPs) that can accurately discriminate homozygous and heterozygous genotypes using microfluidics technology. To achieve this, our system performs real-time melting-curve analysis of surface-immobilized hybridization probes. As an example, we used our sensor to analyze two SNPs in the apolipoprotein E (ApoE) gene, where homozygous and heterozygous mutations greatly affect the risk of late-onset Alzheimer's disease. Using probes specific for each SNP, we simultaneously acquired melting curves for probe-target duplexes at two different loci and thereby accurately distinguish all six possible ApoE allele combinations. Since the design of our device and probes can be readily adapted for targeting other loci, we believe that our method offers a modular platform for the diagnosis of SNP-based diseases and personalized medicine.

摘要

我们报道了首个用于检测单核苷酸多态性(SNP)的电化学系统,该系统利用微流控技术能够准确区分纯合子和杂合子基因型。为实现这一目标,我们的系统对表面固定的杂交探针进行实时熔解曲线分析。例如,我们使用该传感器分析载脂蛋白E(ApoE)基因中的两个SNP,其中纯合子和杂合子突变极大地影响迟发性阿尔茨海默病的风险。使用针对每个SNP的特异性探针,我们同时获取了两个不同位点的探针 - 靶标双链体的熔解曲线,从而准确区分所有六种可能的ApoE等位基因组合。由于我们的设备和探针设计可以很容易地适用于靶向其他位点,我们相信我们的方法为基于SNP的疾病诊断和个性化医疗提供了一个模块化平台。