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用于高通量单分子光学成像的DNA帘幕

DNA curtains for high-throughput single-molecule optical imaging.

作者信息

Greene Eric C, Wind Shalom, Fazio Teresa, Gorman Jason, Visnapuu Mari-Liis

机构信息

Howard Hughes Medical Institute, Columbia University, New York, NY, USA.

出版信息

Methods Enzymol. 2010;472:293-315. doi: 10.1016/S0076-6879(10)72006-1.

Abstract

Single-molecule approaches provide a valuable tool in the arsenal of the modern biologist, and new discoveries continue to be made possible through the use of these state-of-the-art technologies. However, it can be inherently difficult to obtain statistically relevant data from experimental approaches specifically designed to probe individual reactions. This problem is compounded with more complex biochemical reactions, heterogeneous systems, and/or reactions requiring the use of long DNA substrates. Here we give an overview of a technology developed in our laboratory, which relies upon simple micro- or nanofabricated structures in combination with "bio-friendly" lipid bilayers, to align thousands of long DNA molecules into defined patterns on the surface of a microfluidic sample chamber. We call these "DNA curtains," and we have developed several different versions varying in complexity and DNA substrate configuration, which are designed to meet different experimental needs. This novel approach to single-molecule imaging provides a powerful experimental platform that offers the potential for concurrent observation of hundreds or even thousands of protein-DNA interactions in real time.

摘要

单分子方法为现代生物学家提供了一种宝贵的工具,通过使用这些先进技术,新的发现不断成为可能。然而,从专门设计用于探测单个反应的实验方法中获得具有统计学意义的数据,其本质上可能很困难。对于更复杂的生化反应、异质系统和/或需要使用长DNA底物的反应,这个问题会更加复杂。在这里,我们概述了我们实验室开发的一种技术,该技术依靠简单的微纳加工结构与“生物友好型”脂质双层相结合,将数千个长DNA分子排列成微流控样品室表面的特定图案。我们将这些称为“DNA帘”,并且我们已经开发了几种不同版本,其复杂性和DNA底物配置各不相同,旨在满足不同的实验需求。这种新颖的单分子成像方法提供了一个强大的实验平台,具有实时同时观察数百甚至数千个蛋白质-DNA相互作用的潜力。

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