DNA折纸
纳米技术
DNA
DNA纳米技术
脚手架
模板
制作
滚动圆复制
材料科学
化学
纳米结构
DNA复制
计算机科学
数据库
医学
病理
生物化学
替代医学
作者
Alexandria N. Marchi,Ishtiaq Saaem,Briana N. Vogen,Stanley Brown,Thomas H. LaBean
出处
期刊:Nano Letters
[American Chemical Society]
日期:2014-09-01
卷期号:14 (10): 5740-5747
被引量:185
摘要
Structural DNA nanotechnology, and specifically scaffolded DNA origami, is rapidly developing as a versatile method for bottom-up fabrication of novel nanometer-scale materials and devices. However, lengths of conventional single-stranded scaffolds, for example, 7,249-nucleotide circular genomic DNA from the M13mp18 phage, limit the scales of these uniquely addressable structures. Additionally, increasing DNA origami size generates the cost burden of increased staple-strand synthesis. We addressed this 2-fold problem by developing the following methods: (1) production of the largest to-date biologically derived single-stranded scaffold using a λ/M13 hybrid virus to produce a 51 466-nucleotide DNA in a circular, single-stranded form and (2) inexpensive DNA synthesis via an inkjet-printing process on a chip embossed with functionalized micropillars made from cyclic olefin copolymer. We have experimentally demonstrated very efficient assembly of a 51-kilobasepair origami from the λ/M13 hybrid scaffold folded by chip-derived staple strands. In addition, we have demonstrated two-dimensional, asymmetric origami sheets with controlled global curvature such that they land on a substrate in predictable orientations that have been verified by atomic force microscopy.
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