Geometrically programmed self-limited assembly of tubules using DNA origami colloids
Daichi Hayakawa, Thomas E. Videb{\ae}k, Douglas M. Hall, Huang Fang,, Christian Sigl, Elija Feigl, Hendrik Dietz, Seth Fraden, Michael F. Hagan,, Gregory M. Grason, W. Benjamin Rogers

TL;DR
This paper presents a method for designing DNA origami-based subunits that self-assemble into tubules with controllable width and chirality, advancing the creation of self-limited nanostructures for functional materials.
Contribution
It introduces a geometrically programmed approach to self-limiting tubule assembly using DNA origami, including models for predicting tubule dimensions and methods to reduce assembly variability.
Findings
Tubules can reach micrometer lengths with prescribed widths.
Distribution in tubule width and chirality can be modeled considering bending rigidity.
Using multiple subunit species reduces end-state variability.
Abstract
Self-assembly is one of the most promising strategies for making functional materials at the nanoscale, yet new design principles for making self-limiting architectures, rather than spatially unlimited periodic lattice structures, are needed. To address this challenge, we explore the trade-offs between addressable assembly and self-closing assembly of a specific class of self-limiting structures: cylindrical tubules. We make triangular subunits using DNA origami that have specific, valence-limited interactions and designed binding angles, and study their assembly into tubules that have a self-limited width that is much larger than the size of an individual subunit. In the simplest case, the tubules are assembled from a single component by geometrically programming the dihedral angles between neighboring subunits. We show that the tubules can reach many micrometers in length and that…
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Taxonomy
TopicsAdvanced biosensing and bioanalysis techniques · Supramolecular Self-Assembly in Materials · Modular Robots and Swarm Intelligence
