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芯片上无胶电泳 DNA 和蛋白质,采用 70nm 毛细孔图案。

Gel-free electrophoresis of DNA and proteins on chips featuring a 70 nm capillary-well motif.

机构信息

Department of Electronic and Computer Engineering, Hong Kong University of Science and Technology , Clear Water Bay, Kowloon, Hong Kong.

出版信息

ACS Nano. 2015 Jan 27;9(1):427-35. doi: 10.1021/nn505605e. Epub 2014 Dec 26.

Abstract

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 5.6-5.8 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 μm) photolithography and standard semiconductor manufacturing techniques.

摘要

我们提出了一种基于硅的集成玻璃毛细管系统,用于基于大小的筛分不同混合物的蛋白质、短 DNA 和长 DNA 片段,形成尖锐的峰。实现的最小可分辨尺寸差异为 3.45 kDa 的 45-52.8 kDa 蛋白质、20 bp 的 200-300 bp DNA 链和 182 bp 的 5.6-5.8 kbp DNA 链。这种高分辨率筛分源于在极受限(电阻)毛细管段起始处产生的巨大陡峭熵障碍,以及它们在将平衡熵筛分转移到强场(>1000 V/cm)中所起的关键作用。各种大小的 DNA 片段在 2000 V 的稳定电压下不到 7 分钟即可完全分离,该电压直接施加在具有数千个熵障碍的 2 厘米长的筛子的长度上。通过时分复用,在不引发介电击穿的情况下,还展示了更高场强和更长筛子的实用性,可在 1 厘米长的筛子段上施加高达 2000 V 的电压。自封闭的 70nm 直径毛细管使用粗 (>1 μm) 光刻和标准半导体制造技术制造。

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