The Center for Biomedical Engineering and Rehabilitation Science, Louisiana Tech University, P.O. Box 10157/BEC228, 818 Nelson Avenue, Ruston, LA 71272, USA.
Lab Chip. 2011 May 21;11(10):1761-9. doi: 10.1039/c0lc00733a. Epub 2011 Apr 5.
This study describes a novel, thermoelectric method for DNA sequencing in a microfluidic device. The method measures the heat released when DNA polymerase inserts a deoxyribonucleoside triphosphate into a primed DNA template. The study describes the principle of operation of a laminar flow microfluidic chip with a reaction zone that contains DNA template/primer complex immobilized to the inner surface of the device's lower channel wall. A thin-film thermopile attached to the external surface of the lower channel wall measures the dynamic change in temperature that results when Klenow polymerase inserts a deoxyribonucleoside triphosphate into the DNA template. The intrinsic rejection of common-mode thermal signals by the thermopile in combination with hydrodynamic focused flow allows for the measurement of temperature changes on the order of 10(-4) K without control of ambient temperature. To demonstrate the method, we report the sequencing of a model oligonucleotide containing 12 bases. Results demonstrate that it is feasible to sequence DNA by measuring the heat released during nucleotide incorporation. This thermoelectric method for sequencing DNA may offer a novel new method of DNA sequencing for personalized medicine applications.
本研究描述了一种新颖的、在微流控装置中进行 DNA 测序的热电方法。该方法测量 DNA 聚合酶将脱氧核糖核苷三磷酸插入引物 DNA 模板时释放的热量。本研究描述了具有层流微流控芯片的工作原理,该芯片的反应区包含固定在器件下通道壁内表面的 DNA 模板/引物复合物。附着在下通道壁外表面的薄膜热电偶测量当 Klenow 聚合酶将脱氧核糖核苷三磷酸插入 DNA 模板时导致的温度动态变化。热堆对常见模式热信号的固有排斥以及流体动力聚焦流的结合允许在不控制环境温度的情况下测量 10(-4) K 量级的温度变化。为了演示该方法,我们报告了对包含 12 个碱基的模型寡核苷酸的测序。结果表明,通过测量核苷酸掺入过程中释放的热量来进行 DNA 测序是可行的。这种用于 DNA 测序的热电方法可能为个性化医疗应用提供一种新颖的 DNA 测序方法。