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一种用于实时可视化单 DNA 分子水平上 DNA-蛋白质相互作用的纳流控装置。

A nanofluidic device for real-time visualization of DNA-protein interactions on the single DNA molecule level.

机构信息

Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

出版信息

Nanoscale. 2019 Jan 23;11(4):2071-2078. doi: 10.1039/c8nr09023h.

Abstract

Single DNA molecule techniques have revolutionized our understanding of DNA-protein interactions. Traditional techniques for such studies have the major drawback that the DNA molecule studied is attached to a bead or a surface. Stretching of DNA molecules in nanofluidic channels has enabled single-molecule studies of DNA-protein interactions without the need of tethering the molecule to a foreign entity. This in turn allows for studying reactions along the whole extension of the molecule, including the free DNA ends. However, existing studies either rely on measurements where all components are mixed before introduction into the nanochannels or where passive diffusion brings the reagents to the confined DNA molecule. We here present a new generation of nanofluidic devices, where active exchange of the local environment within the nanofluidic channel is possible, while keeping the DNA molecule stretched and in confinement. To demonstrate the functionality of this novel device we added different analytes, such as SDS, spermidine and DNase I, to YOYO-1 stained DNA and studied the response in real time. We also performed a FRET-based reaction, where two different analytes were added sequentially to the same DNA molecule. We believe that this design will enable in situ mapping of complex biochemical processes, involving multiple proteins and cofactors, on single DNA molecules as well as other biomacromolecules.

摘要

单分子 DNA 技术彻底改变了我们对 DNA-蛋白质相互作用的理解。传统的此类研究技术主要存在一个缺陷,即所研究的 DNA 分子附着在珠子或表面上。在纳米流道中拉伸 DNA 分子,可以在无需将分子连接到外部实体的情况下,对 DNA-蛋白质相互作用进行单分子研究。这反过来又可以研究分子整个延伸部分的反应,包括游离的 DNA 末端。然而,现有的研究要么依赖于所有成分在引入纳米通道之前混合的测量,要么依赖于被动扩散将试剂带到受限的 DNA 分子上。我们在这里展示了新一代的纳米流体设备,在保持 DNA 分子拉伸和受限的同时,能够在纳米流体通道内进行局部环境的主动交换。为了证明这种新型设备的功能,我们向 YOYO-1 染色的 DNA 中添加了不同的分析物,如 SDS、亚精胺和 DNA 酶 I,并实时研究了其响应。我们还进行了基于 FRET 的反应,其中将两种不同的分析物依次添加到同一 DNA 分子上。我们相信,这种设计将能够在单个 DNA 分子以及其他生物大分子上原位映射涉及多种蛋白质和辅助因子的复杂生化过程。

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