DNA折纸
化学
DNA
脚手架
核酸外切酶 III
纳米技术
纳米结构
DNA纳米技术
生物物理学
组合化学
生物化学
基因
材料科学
医学
大肠杆菌
生物
生物医学工程
作者
Willem E. M. Noteborn,Leoni Abendstein,Thomas H. Sharp
标识
DOI:10.1021/acs.bioconjchem.0c00644
摘要
DNA origami nanostructures generally require a single scaffold strand of specific length, combined with many small staple strands. Ideally, the length of the scaffold strand should be dictated by the size of the designed nanostructure. However, synthesizing arbitrary-length single-stranded DNA in sufficient quantities is difficult. Here, we describe a straightforward and accessible method to produce defined-length ssDNA scaffolds using PCR and subsequent selective enzymatic digestion with T7 exonuclease. This approach produced ssDNA with higher yields than other methods and without the need for purification, which significantly decreased the time from PCR to obtaining pure DNA origami. Furthermore, this enabled us to perform true one-pot synthesis of defined-size DNA origami nanostructures. Additionally, we show that multiple smaller ssDNA scaffolds can efficiently substitute longer scaffolds in the formation of DNA origami.
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