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基于剪切的工程化 DNA 纳米开关的 LC 纯化及其对 DNA 折纸的启示。

Shear Dependent LC Purification of an Engineered DNA Nanoswitch and Implications for DNA Origami.

机构信息

The RNA Institute, University at Albany, State University of New York , 1400 Washington Avenue, Albany, New York 12222, United States.

Department of Chemistry and Chemical Biology and the Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute , 110 Eighth Street, Troy, New York 12180, United States.

出版信息

Anal Chem. 2017 Jun 6;89(11):5673-5677. doi: 10.1021/acs.analchem.7b00791. Epub 2017 May 8.

DOI:10.1021/acs.analchem.7b00791
PMID:28474522
Abstract

As DNA nanotechnology matures, there is increasing need for fast, reliable, and automated purification methods. Here, we develop UHPLC methods to purify self-assembled DNA nanoswitches, which are formed using DNA origami approaches and are designed to change conformations in response to a binding partner. We found that shear degradation hindered LC purification of the DNA nanoswitches, removing oligonucleotides from the scaffold strand and causing loss of function. However, proper choice of column, flow rate, and buffers enabled robust and automated purification of DNA nanoswitches without loss of function in under a half hour. Applying our approach to DNA origami structures, we found that ∼400 nm long nanotubes degraded under the gentlest flow conditions while ∼40 nm diameter nanospheres remained intact even under aggressive conditions. These examples show how fluid stresses can affect different DNA nanostructures during LC purification and suggest that shear forces may be relevant for some applications of DNA nanotechnology. Further development of this approach could lead to fast and automated purification of DNA nanostructures of various shapes and sizes, which would be an important advance for the field.

摘要

随着 DNA 纳米技术的成熟,人们越来越需要快速、可靠和自动化的纯化方法。在这里,我们开发了 UHPLC 方法来纯化自组装的 DNA 纳米开关,这些开关是使用 DNA 折纸方法形成的,旨在响应结合伴侣改变构象。我们发现,剪切降解会阻碍 DNA 纳米开关的 LC 纯化,从支架链上除去寡核苷酸,并导致功能丧失。然而,适当选择柱、流速和缓冲液可以在不到半小时的时间内实现 DNA 纳米开关的稳健和自动化纯化,而不会丧失功能。将我们的方法应用于 DNA 折纸结构,我们发现即使在剧烈的条件下,约 400nm 长的纳米管在最温和的流动条件下也会降解,而约 40nm 直径的纳米球仍然完整。这些例子表明,在 LC 纯化过程中流体应力如何影响不同的 DNA 纳米结构,并表明剪切力可能与 DNA 纳米技术的某些应用相关。这种方法的进一步发展可能会导致各种形状和大小的 DNA 纳米结构的快速和自动化纯化,这将是该领域的重要进展。

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