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A Patch-Clamp ASIC for Nanopore-Based DNA Analysis

机译:膜片钳ASIC,用于基于纳米孔的DNA分析

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In this paper, a fully integrated high-sensitivity patch-clamp system is proposed for single-molecule deoxyribonucleic acid (DNA) analysis using a nanopore sensor. This system is composed of two main blocks for amplification and compensation. The amplification block is composed of three stages: 1) a headstage, 2) a voltage-gain difference amplifier, and 3) a track-and-hold circuit, that amplify a minute ionic current variation sensed by the nanopore while the compensation block avoids the headstage saturation caused by the input parasitic capacitances during sensing. By employing design techniques novel for this application, such as an instrumentation—amplifier topology and a compensation switch, we minimize the deleterious effects of the input-offset voltage and the input parasitic capacitances while attaining hardware simplicity. This system is fabricated in a 0.35 $mu$ m 4M2P CMOS process and is demonstrated using an $alpha$-hemolysin protein nanopore for detection of individual molecules of single-stranded DNA that pass through the 1.5 nm-diameter pore. In future work, the refined system will functionalize single and multiple solid-state nanopores formed in integrated microfluidic devices for advanced DNA analysis, in scientific and diagnostic applications.
机译:本文提出了一种完全集成的高灵敏度膜片钳系统,用于使用纳米孔传感器对单分子脱氧核糖核酸(DNA)进行分析。该系统由两个主要模块组成,分别用于放大和补偿。放大模块由三个阶段组成:1)前级; 2)电压增益差动放大器; 3)跟踪保持电路,可放大由纳米孔感测的微小离子电流变化,而补偿模块则避免了感测期间由输入寄生电容引起的前端饱和。通过采用针对该应用的新颖设计技术(例如仪表放大器拓扑和补偿开关),我们在使硬件简化的同时,最大程度地减小了输入失调电压和输入寄生电容的有害影响。该系统采用0.35 $ mu $ m 4M2P CMOS工艺制造,并使用 $ alpha $ -溶血素蛋白纳米孔,用于检测穿过1.5纳米直径孔的单链DNA的单个分子。在未来的工作中,经过改进的系统将功能化在集成微流体设备中形成的单个和多个固态纳米孔,以在科学和诊断应用中进行高级DNA分析。

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