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在直流电场下通过石英纳米柱芯片分离长链DNA分子。

Separation of long DNA molecules by quartz nanopillar chips under a direct current electric field.

作者信息

Kaji Noritada, Tezuka Yojiro, Takamura Yuzuru, Ueda Masanori, Nishimoto Takahiro, Nakanishi Hiroaki, Horiike Yasuhiro, Baba Yoshinobu

机构信息

Department of Medicinal Chemistry, Faculty of Pharmaceutical Sciences, The University of Tokushima, CREST, Japan.

出版信息

Anal Chem. 2004 Jan 1;76(1):15-22. doi: 10.1021/ac030303m.

Abstract

We have established the nanofabrication technique for constructing nanopillars with high aspect ratio (100-500 nm diameter and 500-5000 nm tall) inside a microchannel on a quartz chip. The size of pillars and the spacing between pillars are designed as a DNA sieving matrix for optimal analysis of large DNA fragments over a few kilobase pairs (kbp). A chip with nanopillar channel and simple cross injector was developed based on the optimal design and applied to the separation of DNA fragments (1-38 kbp) and large DNA fragments (lambda DNA, 48.5 kbp; T4 DNA, 165.6 kbp) that are difficult to separate on conventional gel electrophoresis and capillary electrophoresis without a pulsed-field technique. DNA fragments ranging from 1 to 38 kbp were separated as clear bands, and furthermore, the mixture of lambda DNA and T4 DNA was successfully separated by a 380-microm-long nanopillar channel within only 10 s even under a direct current (dc) electric field. Theoretical plate number N of the channel (380-1450 microm long) was 1000-3000 (0.7 x 10(6)-2.1 x 10(6) plates/m). A single DNA molecule observation during electrophoresis in a nanopillar channel revealed that the optimal nanopillars induced T4 DNA to form a narrow U-shaped conformation during electrophoresis whereas lambda DNA kept a rather spherical conformation. We demonstrated that, even under a dc electric field, the optimal nanopillar dimensions depend on a gyration radius of DNA molecule that made it possible to separate large DNA fragments in a short time.

摘要

我们已经建立了一种纳米制造技术,用于在石英芯片上的微通道内构建具有高纵横比的纳米柱(直径100 - 500 nm,高500 - 5000 nm)。柱的尺寸和柱间距被设计为一种DNA筛分基质,用于对几千碱基对(kbp)以上的大DNA片段进行优化分析。基于这种优化设计,开发了一种带有纳米柱通道和简单交叉注射器的芯片,并将其应用于DNA片段(1 - 38 kbp)以及大DNA片段(λDNA,48.5 kbp;T4 DNA,165.6 kbp)的分离,这些大DNA片段在没有脉冲场技术的情况下,在传统凝胶电泳和毛细管电泳中很难分离。1至38 kbp的DNA片段被分离成清晰的条带,此外,即使在直流(dc)电场下,λDNA和T4 DNA的混合物也能通过一个380微米长的纳米柱通道在仅10秒内成功分离。该通道(380 - 1450微米长)的理论塔板数N为1000 - 3000(0.7×10⁶ - 2.1×10⁶ 块/米)。在纳米柱通道中进行电泳时对单个DNA分子的观察表明,优化后的纳米柱在电泳过程中诱导T4 DNA形成狭窄的U形构象,而λDNA则保持相当球形的构象。我们证明,即使在直流电场下,优化后的纳米柱尺寸取决于DNA分子的回转半径,这使得在短时间内分离大DNA片段成为可能。

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