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双链 DNA 作为统一支架的 DNA 折纸术。

DNA origami with double-stranded DNA as a unified scaffold.

机构信息

Department of Chemistry and Biochemistry & The Biodesign Institute, Arizona State University, Tempe, Arizona 85287, United States.

出版信息

ACS Nano. 2012 Sep 25;6(9):8209-15. doi: 10.1021/nn302896c. Epub 2012 Jul 27.

DOI:10.1021/nn302896c
PMID:22830653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3654836/
Abstract

Scaffolded DNA origami is a widely used technology for self-assembling precisely structured nanoscale objects that contain a large number of addressable features. Typical scaffolds are long, single strands of DNA (ssDNA) that are folded into distinct shapes through the action of many, short ssDNA staples that are complementary to several different domains of the scaffold. However, sources of long single-stranded DNA are scarce, limiting the size and complexity of structures that can be assembled. Here we demonstrated that dsDNA (double-stranded DNA) scaffolds can be directly used to fabricate integrated DNA origami structures that incorporate both of the constituent ssDNA molecules. Two basic principles were employed in the design of scaffold folding paths: folding path asymmetry and periodic convergence of the two ssDNA scaffold strands. Asymmetry in the folding path minimizes unwanted complementarity between staples, and incorporating an offset between the folding paths of each ssDNA scaffold strand reduces the number of times that complementary portions of the strands are brought into close proximity with one another, both of which decrease the likelihood of dsDNA scaffold recovery. Meanwhile, the folding paths of the two ssDNA scaffold strands were designed to periodically converge to promote the assembly of a single, unified structure rather than two individual ones. Our results reveal that this basic strategy can be used to reliably assemble integrated DNA nanostructures from dsDNA scaffolds.

摘要

有支架的 DNA 折纸术是一种广泛使用的技术,可用于自组装具有大量可寻址特征的精确结构的纳米级物体。典型的支架是长的单链 DNA(ssDNA),通过许多短的 ssDNA 订书钉的作用折叠成不同的形状,这些短的 ssDNA 订书钉与支架的几个不同域互补。然而,长单链 DNA 的来源稀缺,限制了可以组装的结构的大小和复杂性。在这里,我们证明了 dsDNA(双链 DNA)支架可以直接用于制造整合的 DNA 折纸结构,该结构包含两个组成的 ssDNA 分子。在支架折叠路径的设计中采用了两个基本原则:折叠路径的不对称性和两条 ssDNA 支架链的周期性收敛。折叠路径的不对称性最小化了订书钉之间不必要的互补性,并且在每个 ssDNA 支架链的折叠路径之间引入偏移会减少互补链部分彼此紧密接近的次数,这两种情况都降低了 dsDNA 支架恢复的可能性。同时,两条 ssDNA 支架链的折叠路径被设计为周期性收敛,以促进单个统一结构的组装,而不是两个独立结构的组装。我们的结果表明,这种基本策略可用于从 dsDNA 支架可靠地组装集成的 DNA 纳米结构。

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