4.8 Article

Developmental Self-Assembly of a DNA Tetrahedron

Journal

ACS NANO
Volume 8, Issue 4, Pages 3251-3259

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn4038223

Keywords

molecular programming; DNA nanotechnology; kinetic pathway control; developmental self-assembly

Funding

  1. Office of Naval Research [N000141010827, N000141310593, N000141110914]
  2. NSF CAREER Award [CCF1054898]
  3. NSF [CCF1162459, CCF1317291]
  4. Wyss Institute for Biologically Inspired Engineering Faculty Startup Fund
  5. NIH [5R01CA140759, P50 HG004071, 1K99EB015331, 1DP2OD007292]
  6. Molecular Programming Project [NSF-CCF-0832824, NSF-CCF-1317694]
  7. Gordon and Betty Moore Foundation [GBMF2809]
  8. Buttonwood Foundation
  9. Division of Computing and Communication Foundations
  10. Direct For Computer & Info Scie & Enginr [0832824, 1317694] Funding Source: National Science Foundation

Ask authors/readers for more resources

Kinetically controlled isothermal growth is fundamental to biological development, yet it remains challenging to rationally design molecular systems that self-assemble isothermally into complex geometries via prescribed assembly and disassembly pathways. By exploiting the programmable chemistry of base pairing, sophisticated spatial and temporal control have been demonstrated in DNA self-assembly, but largely as separate pursuits. By integrating temporal with spatial control, here we demonstrate the developmental self-assembly of a DNA tetrahedron, where a prescriptive molecular program orchestrates the kinetic pathways by which DNA molecules isothermally self-assemble into a well-defined three-dimensional wireframe geometry. In this reaction, nine DNA reactants initially coexist metastably, but upon catalysis by a DNA initiator molecule, navigate 24 individually characterizable intermediate states via prescribed assembly pathways, organized both in series and In parallel, to arrive at the tetrahedral final product. In contrast to previous work on dynamic DNA nanotechnology, this developmental program coordinates growth of ringed substructures into a three-dimensional wireframe superstructure, taking a step toward the goal of kinetically controlled isothermal growth of complex three-dimensional geometries.

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