Rapid and High-Yielding Purification of DNA Self-Assembled Structures by Aqueous Two-Phase System.

Q4 Biochemistry, Genetics and Molecular Biology Methods in molecular biology Pub Date : 2025-01-01 DOI:10.1007/978-1-0716-4394-5_2
Marcos K Masukawa, Masahiro Takinoue
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Abstract

Aqueous two-phase systems (ATPS) of dextran and polyethylene glycol (PEG) enable the purification of DNA structures such as DNA origami and DNA nanotubes in times as short as 10 min. This method, which has recovery yields >90% for a typical DNA origami, owes its efficiency to the highly selective partition of the DNA structures in the dextran phase of these emulsions. This purification method is carried out in conditions that promote the structural stability of these structures, making it particularly suitable for DNA nanotechnology. In this protocol, we will describe the materials and methods for purifying DNA origami and quantifying the purification yield by agarose electrophoresis and image analysis.

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利用水性两相系统快速高产地纯化 DNA 自组装结构
葡聚糖和聚乙二醇(PEG)的水两相体系(ATPS)可以在短至10分钟的时间内纯化DNA结构,如DNA折纸和DNA纳米管。这种方法对典型的DNA折纸的回收率为90%,其效率归功于这些乳液中葡聚糖相DNA结构的高度选择性分割。这种纯化方法是在促进这些结构的结构稳定性的条件下进行的,使其特别适合于DNA纳米技术。在本协议中,我们将描述纯化DNA折纸的材料和方法,并通过琼脂糖电泳和图像分析定量纯化产量。
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来源期刊
Methods in molecular biology
Methods in molecular biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.00
自引率
0.00%
发文量
3536
期刊介绍: For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.
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