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Gel-Free Electrophoresis of DNA and Proteins on Chips Featuring a 70 nm Capillary-Well Motif

机译:芯片上具有70 nm毛细孔母体的DNA和蛋白质的无凝胶电泳

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摘要

We present an integrated glass capillary system on silicon for size-based sieving of distinct mixtures of proteins, short DNA, and long DNA fragments into sharp peaks. The minimum resolvable size difference achieved is noted as 3.45 kDa for 45-52.8 kDa proteins, 20 bp for 200-300 bp DNA strands, and 182 bp for 5.65.8 kbp DNA chains. This high-resolution sieving arises from vastly steep entropic barriers created at the onsets of extremely restrictive (resistive) capillary segments and their pivotal role in shifting the equilibrium entropic sieving to intense fields (>1000 V/cm). DNA fragments of various sizes are shown fully resolved in less than 7 min at a steady voltage of 2000 V being directly applied across the length of a 2 cm long sieve featuring thousands of entropic barriers. The utility of higher field strengths and longer sieves is also demonstrated without triggering dielectric breakdown by time-division multiplexing up to 2000 V across the 1 cm long sieve segments. The self-enclosed 70 nm diameter capillaries were fabricated using coarse (>1 mu m) photolithography and standard semiconductor manufacturing techniques.
机译:我们提出了一种基于硅的集成玻璃毛细管系统,用于将蛋白质,短DNA和长DNA片段的独特混合物按大小进行筛分,形成尖锐的峰。对于45-52.8 kDa的蛋白质,达到的最小可分辨大小差异为3.45 kDa,对于200-300 bp的DNA链为20 bp,对于5.65.8 kbp的DNA链为182 bp。这种高分辨率的筛分是由于在限制性极强(阻性)毛细管段开始时产生的非常陡峭的熵垒及其在将平衡熵筛分转移到强磁场(> 1000 V / cm)中的关键作用。各种大小的DNA片段显示在不到2000分钟的稳定电压下,在不到7分钟的时间内即可完全分解,并直接施加在具有数千个熵屏障的2 cm长筛子的整个长度上。还通过在1 cm长的筛网段上时分多路复用高达2000 V的时分多路复用,证明了更高的场强和更长的筛子的效用而不会触发介电击穿。自封闭的直径为70 nm的毛细管是使用粗糙(> 1μm)光刻技术和标准半导体制造技术制造的。

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