Symmetry-Guided Inverse Design of Self-Assembling Multiscale DNA Origami Tilings.

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY ACS Nano Pub Date : 2024-07-23 Epub Date: 2024-07-09 DOI:10.1021/acsnano.4c04515
Daichi Hayakawa, Thomas E Videbæk, Gregory M Grason, W Benjamin Rogers
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Abstract

Recent advances enable the creation of nanoscale building blocks with complex geometries and interaction specificities for self-assembly. This nearly boundless design space necessitates design principles for defining the mutual interactions between multiple particle species to target a user-specified complex structure or pattern. In this article, we develop a symmetry-based method to generate the interaction matrices that specify the assembly of two-dimensional tilings, which we illustrate using equilateral triangles. By exploiting the allowed 2D symmetries, we develop an algorithmic approach by which any periodic 2D tiling can be generated from an arbitrarily large number of subunit species, notably addressing an unmet challenge of engineering 2D crystals with periodicities that can be arbitrarily larger than the subunit size. To demonstrate the utility of our design approach, we encode specific interactions between triangular subunits synthesized by DNA origami and show that we can guide their self-assembly into tilings with a wide variety of symmetries, using up to 12 unique species of triangles. By conjugating specific triangles with gold nanoparticles, we fabricate gold-nanoparticle supracrystals whose lattice parameter spans up to 300 nm. Finally, to generate economical design rules, we compare the design economy of various tilings. In particular, we show that (1) higher symmetries allow assembly of larger unit cells with fewer subunits and (2) linear supracrystals can be designed more economically using linear primitive unit cells. This work provides a simple algorithmic approach to designing periodic assemblies, aiding in the multiscale assembly of supracrystals of nanostructured "meta-atoms" with engineered plasmonic functions.

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对称性引导下的自组装多尺度 DNA 折纸叠层逆向设计
最近的技术进步使人们能够创造出具有复杂几何形状和相互作用特异性的纳米级构件,从而实现自组装。这种近乎无边无际的设计空间需要设计原则来定义多种粒子之间的相互作用,以实现用户指定的复杂结构或模式。在这篇文章中,我们开发了一种基于对称性的方法来生成相互作用矩阵,以指定二维斜面的组装,我们用等边三角形来说明这一点。通过利用允许的二维对称性,我们开发了一种算法方法,通过这种方法可以从任意数量的亚单位种类生成任何周期性的二维平铺,从而显著解决了工程二维晶体周期性可任意大于亚单位尺寸这一尚未解决的难题。为了证明我们的设计方法的实用性,我们对通过 DNA 折纸合成的三角形亚基之间的特定相互作用进行了编码,结果表明,我们可以利用多达 12 种独特的三角形,引导它们自组装成具有多种对称性的层叠结构。通过将特定三角形与金纳米粒子共轭,我们制造出了晶格参数跨度达 300 纳米的金纳米粒子超晶体。最后,为了生成经济的设计规则,我们比较了各种三角形的设计经济性。特别是,我们发现:(1) 较高的对称性允许用较少的子单元组装较大的单元格;(2) 使用线性原始单元格可以更经济地设计线性超晶体。这项研究为设计周期性组装提供了一种简单的算法方法,有助于多尺度组装具有工程质子功能的纳米结构 "元原子 "超晶体。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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