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可调谐限制实现单细胞操作与单分子 DNA 线性化的桥接。

Tunable Confinement for Bridging Single-Cell Manipulation and Single-Molecule DNA Linearization.

机构信息

Department of Mechanical and Aerospace Engineering, The Hong Kong University of Science and Technology, Kowloon, 999077, Hong Kong, China.

Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Kowloon, 999077, Hong Kong, China.

出版信息

Small. 2018 Apr;14(17):e1800229. doi: 10.1002/smll.201800229. Epub 2018 Mar 25.

DOI:10.1002/smll.201800229
PMID:29575689
Abstract

DNA linearization by nanoconfinement has offered a new avenue toward large-scale genome mapping. The ability to smoothly interface the widely different length scales from cell manipulation to DNA linearization is critical to the development of single-cell genomic mapping or sequencing technologies. Conventional nanochannel technologies for DNA analysis suffer from complex fabrication procedures, DNA stacking at the nanochannel entrance, and inefficient solution exchange. In this work, a dynamic and tunable confinement strategy is developed to manipulate and linearize genomic-length DNA molecules from a single cell. By leveraging pneumatic microvalve control and elastomeric collapse, an array of nanochannels with confining dimension down to 20 nm and length up to sub-millimeter is created and can be dynamically tuned in size. The curved edges of the microvalve form gradual transitions from microscale to nanoscale confinement, smoothly facilitating DNA entry into the nanochannels. A unified micro/nanofluidic device that integrates single-cell trapping and lysis, DNA extraction, purification, labeling, and linearization is developed based on dynamically controllable nanochannels. Mbp-long DNA molecules are extracted directly from a single cell and in situ linearized in the nanochannels. The device provides a facile and promising platform to achieve the ultimate goal of single-cell, single-genome analysis.

摘要

纳米限域使 DNA 线性化,为大规模基因组图谱绘制提供了新途径。能够顺利地将从细胞操作到 DNA 线性化的广泛不同的长度尺度进行接口,这对单细胞基因组图谱绘制或测序技术的发展至关重要。传统的用于 DNA 分析的纳米通道技术存在复杂的制造工艺、纳米通道入口处的 DNA 堆积以及低效的溶液交换等问题。在这项工作中,开发了一种动态可调的限域策略,用于从单个细胞中操作和线性化基因组长度的 DNA 分子。通过利用气动微阀控制和弹性体的坍塌,可以创建具有 20nm 以下限域尺寸和亚毫米级长度的纳米通道阵列,并可以动态地进行尺寸调节。微阀的弯曲边缘形成从微尺度到纳米尺度限域的逐渐过渡,从而顺利地促进 DNA 进入纳米通道。基于动态可控纳米通道,开发了一种集成单细胞捕获和裂解、DNA 提取、纯化、标记和线性化的微纳流控装置。从单个细胞中直接提取长达 Mbp 的 DNA 分子,并在纳米通道中就地线性化。该装置提供了一个简单而有前途的平台,以实现单细胞、单基因组分析的最终目标。

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