Yang Allen H J, Hsieh Kuangwen, Patterson Adriana S, Ferguson B Scott, Eisenstein Michael, Plaxco Kevin W, Soh H Tom
Department of Mechanical Engineering, University of California Santa Barbara (USA).
Angew Chem Int Ed Engl. 2014 Mar 17;53(12):3163-7. doi: 10.1002/anie.201310059. Epub 2014 Feb 12.
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.
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。