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Melting analysis on microbeads in rapid temperature-gradient inside microchannels for single nucleotide polymorphisms detection

机译:微通道内部快速温度梯度微珠的熔解分析用于单核苷酸多态性检测

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摘要

A continuous-flow microchip with a temperature gradient in microchannels was utilized to demonstrate spatial melting analysis on microbeads for clinical Single Nucleotide Polymorphisms (SNPs) genotyping on animal genomic DNA. The chip had embedded heaters and thermometers, which created a rapid and yet stable temperature gradient between 60 °C and 85 °C in a short distance as the detection region. The microbeads, which served as mobile supports carrying the target DNA and fluorescent dye, were transported across the temperature gradient. As the surrounding temperature increased, the fluorescence signals of the microbeads decayed with this relationship being acquired as the melting curve. Fast DNA denaturation, as a result of the improved heat transfer and thermal stability due to scaling, was also confirmed. Further, each individual microbead could potentially bear different sequences and pass through the detection region, one by one, for a series of melting analysis, with multiplex, high-throughput capability being possible. A prototype was tested with target DNA samples in different genotypes (i.e., wild and mutant types) with a SNP location from Landrace sows. The melting temperatures were obtained and compared to the ones using a traditional tube-based approach. The results showed similar levels of SNP discrimination, validating our proposed technique for scanning homozygotes and heterozygotes to distinguish single base changes for disease research, drug development, medical diagnostics, agriculture, and animal production.
机译:利用在微通道中具有温度梯度的连续流动微芯片,对动物基因组DNA上临床单核苷酸多态性(SNPs)基因型的微珠进行了空间融解分析。该芯片具有嵌入式加热器和温度计,在短距离内作为检测区域,可在60°C至85°C之间产生快速而稳定的温度梯度。微珠作为携带目标DNA和荧光染料的移动载体,在温度梯度范围内运输。随着周围温度的升高,微珠的荧光信号衰减,并以此关系作为熔融曲线。还证实了快速的DNA变性,这是由于结垢改善了热传递和热稳定性的结果。此外,每个单独的微珠可能具有不同的序列,并一个接一个地通过检测区域,以进行一系列的熔解分析,并具有多重,高通量的能力。用具有不同基因型(即野生型和突变型)的靶DNA样品(来自Landrace母猪的SNP位置)测试了原型。获得了熔化温度并将其与使用传统的基于管的方法进行比较。结果显示出相似的SNP鉴别水平,验证了我们提出的扫描纯合子和杂合子的技术,以区分疾病研究,药物开发,医学诊断,农业和动物生产的单一碱基变化。

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