Liedl Tim, Simmel Friedrich C
Department Physik and Center for Nanoscience, LMU Munich, Geschwister-Scholl-Platz 1, 80539 Munich, Germany.
Anal Chem. 2007 Jul 15;79(14):5212-6. doi: 10.1021/ac070242i. Epub 2007 Jun 12.
For fast and reliable determination of DNA melting temperatures with single-nucleotide resolution in a microfluidic setup, stable gradients of the denaturing agent formamide were generated by means of diffusion. Formamide lowers the melting temperature of DNA, and a given formamide concentration can be mapped to a corresponding virtual temperature along the formamide gradient. We applied this concept to determine the melting temperatures of five sets of dye- and quencher-labeled oligonucleotides of different lengths. Differences in the length of complementary sequences of only one nucleotide as well as a single nucleotide mismatch can be detected with this method. Comparison with conventional melting temperature measurements based on temperature scans yields very good agreement.
为了在微流控装置中以单核苷酸分辨率快速可靠地测定DNA熔解温度,通过扩散产生变性剂甲酰胺的稳定梯度。甲酰胺会降低DNA的熔解温度,并且给定的甲酰胺浓度可以沿着甲酰胺梯度映射到相应的虚拟温度。我们应用这一概念来测定五组不同长度的染料和淬灭剂标记的寡核苷酸的熔解温度。该方法可以检测仅一个核苷酸的互补序列长度差异以及单个核苷酸错配。与基于温度扫描的传统熔解温度测量结果相比,一致性非常好。