Automated Synthesis of DNA Nanostructures

Author:

Islas Patricia1ORCID,Platnich Casey M.1ORCID,Gidi Yasser1,Karimi Ryan1ORCID,Ginot Lorianne1,Saliba Daniel1,Luo Xin1,Cosa Gonzalo1ORCID,Sleiman Hanadi F.1ORCID

Affiliation:

1. Department of Chemistry McGill University 801 Sherbrooke Street West Montreal QC H3A 0B8 Canada

Abstract

AbstractDNA nanotechnology has revolutionized the ability to position matter at the nanoscale, but the preparation of DNA‐based architectures remains laborious. To facilitate the formation of custom structures, a fully automated method is reported to produce sequence‐ and size‐defined DNA nanotubes. By programming the sequential addition of desired building blocks, rigid DX‐tile‐based DNA nanotubes and flexible wireframe DNA structures are attained, where the total number of possible constructs increases as a power function of the number of different units available. Using single‐molecule fluorescence imaging, the kinetics and yield of each synthetic step can be quantitatively determined, revealing differences in self‐assembly dynamics as the nanotube is built up from the solid support and providing new insights into DNA self‐assembly. The exploitation of automation for both assembly and analysis (through an ad‐hoc developed K‐means clustering algorithm) facilitates a workflow wherein the synthesis parameters may be iteratively improved upon, demonstrating how a single‐molecule “assembly‐analysis‐optimization” sequence can be used to generate complex, noncovalent materials in good yield. The presented synthetic strategy is generalizable, making use of equipment already available in most standard laboratories and represents the first fully automated supramolecular assembly on a solid support.

Funder

Canada Research Chairs

Canada Foundation for Innovation

Natural Sciences and Engineering Research Council of Canada

Fonds de recherche du Québec – Nature et technologies

Publisher

Wiley

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