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Development of a new technique for DNA single base pair mismatch analysis

机译:DNA单碱基对错配分析新技术的开发

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Research on the development and progression of diseases has shown that single base pair mismatches in key genes can be associated with increased risk of particular cancers. Analytical techniques for determining these mismatches currently exist, but faster, simpler, and cheaper techniques are desirable. We present a new technique based upon DNA melting curve analysis using a temperature gradient established using a silicon wafer. Along one edge of a square silicon substrate, two electrical connectors are mounted to deliver electrical current from a power supply. Since both edge connectors are on the same side of the square, the current flow in the silicon substrate is highest near the edge with the connectors, and decreases as the distance from that edge increases. This non-uniform current distribution generates resistive heating in a manner which, when combined with thermal conductivity effects, results in a nearly linear gradient of measured temperature along the axis normal to the electrode mounting edge. Finite element modeling analysis confirms the results measured with infrared thermal imaging. Using a control loop consisting of a PID controller and an RTD to monitor temperature, gradients of varying temperature ranges can be established. For example, we have routinely created gradients of 0.3/spl deg/C per millimeter for the temperature range of 50 to 70/spl deg/C, with which we have experimentally shown that single base pair mismatches in a section of a commonly studied gene (N-ras gene) can be distinguished from sections which do not contain the mismatch.
机译:对疾病发展和进程的研究表明,关键基因中的单碱基对错配可能与特定癌症的风险增加有关。当前存在用于确定这些失配的分析技术,但是期望更快,更简单和更便宜的技术。我们提出了一种基于DNA熔解曲线分析的新技术,该技术使用了使用硅晶片建立的温度梯度。沿着方形硅基板的一个边缘,安装了两个电连接器,以从电源传输电流。由于两个边缘连接器都位于正方形的同一侧,因此硅基板中的电流在具有连接器的边缘附近最高,并且随着与该边缘的距离增加而减小。这种不均匀的电流分布会以某种方式产生电阻加热,当与导热效果结合使用时,会导致测量温度沿着垂直于电极安装边缘的轴几乎呈线性梯度。有限元建模分析证实了使用红外热成像仪测得的结果。使用由PID控制器和RTD组成的控制回路来监视温度,可以建立不同温度范围的梯度。例如,对于50至70 / spl deg / C的温度范围,我们通常创建每毫米0.3 / spl deg / C的梯度,通过该实验,我们已经证明了在一个共同研究的基因的一部分中单碱基对不匹配(N-ras基因)可以与不包含错配的部分区分开。

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