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DNA合成的电学检测方法的比较分析

Comparative analysis of electrical detection methods of DNA synthesis.

作者信息

Ahn Jinhong, Kim Seok Hyang, Woo Jun-Myung, Park Young June

机构信息

Nano Systems Institute (NSI), Seoul National University, Seoul 151-742, Korea.

出版信息

J Nanosci Nanotechnol. 2012 Jul;12(7):5125-31. doi: 10.1166/jnn.2012.6386.

Abstract

The incorporation of a complementary deoxynucleotide (dNTP) into a self-primed single-stranded DNA (ssDNA) attached to the surface of a sensor electrode generates an H+ charge that can be either trapped on the sensor surface or diffused into the surrounding solution. Electrical detection methods of DNA synthesis are based on these H+ kinetic mechanisms. The detection method that uses ISFET, which is related to the surface trapping mechanism, showed a better sensing signal than the induced charge detection method, which is related to the diffusion of H+ into the surrounding solution. The trapping reaction should be well-controlled, however, so that it would be stable under various surface conditions and temperatures. Moreover, the reaction should be reversible, and the reaction parameters should be well-sustained in the subsequent synthesis cycles. For the induced charge method, the AC current level was too small to be detected using an ordinary amplifier circuit with the same sensor size as that of ISFET. Consequently, the sensor operation sustainability and signal-to-noise ratio characteristics should be addressed carefully in the selection of the proper sensor type.

摘要

将互补脱氧核苷酸(dNTP)掺入附着在传感器电极表面的自引发单链DNA(ssDNA)中会产生H⁺电荷,该电荷既可以捕获在传感器表面,也可以扩散到周围溶液中。DNA合成的电学检测方法基于这些H⁺动力学机制。使用与表面捕获机制相关的离子敏感场效应晶体管(ISFET)的检测方法,比与H⁺扩散到周围溶液相关的感应电荷检测方法显示出更好的传感信号。然而,捕获反应应得到良好控制,以便在各种表面条件和温度下都稳定。此外,反应应该是可逆的,并且反应参数在随后的合成循环中应得到良好维持。对于感应电荷方法,交流电流水平太小,无法使用与ISFET尺寸相同的普通放大器电路进行检测。因此,在选择合适的传感器类型时,应仔细考虑传感器操作的可持续性和信噪比特性。

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