4.8 Article

The influence of Holliday junction sequence and dynamics on DNA crystal self-assembly

Journal

NATURE COMMUNICATIONS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-022-30779-6

Keywords

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Funding

  1. U.S. Department of Energy (DOE), Office of Biological and Environmental Research [DE-AC02-06CH11357]
  2. Howard Hughes Medical Institute
  3. DOE Office of Science User Facility [DE-AC02-05CH11231]
  4. NIH, National Institute of General Medical Sciences (NIGMS) [P30 GM124169]
  5. DOE Office of Science by Brookhaven National Laboratory [DE-SC0012704]
  6. NIH, NIGMS [P41GM111244]
  7. National Science Foundation Division of Materials Research [NSF2004250]
  8. DOE Office of Biological and Environmental Research [KP1605010]
  9. ERDF [CZ.02.1.01/0.0/0.0/15_003/0000477]
  10. Czech Science Foundation [21-23718S]
  11. Arizona State University.
  12. Presidential Strategic Initiative Fund from Arizona State University

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Engineered crystal architectures from DNA have become a foundational goal for nanotechnological precise arrangement. Here, the authors systematically investigate the structures of 36 immobile Holliday junction sequences and identify the features allowing the crystallisation of most of them, while 6 are considered fatal.
The programmable synthesis of rationally engineered crystal architectures for the precise arrangement of molecular species is a foundational goal in nanotechnology, and DNA has become one of the most prominent molecules for the construction of these materials. In particular, branched DNA junctions have been used as the central building block for the assembly of 3D lattices. Here, crystallography is used to probe the effect of all 36 immobile Holliday junction sequences on self-assembling DNA crystals. Contrary to the established paradigm in the field, most junctions yield crystals, with some enhancing the resolution or resulting in unique crystal symmetries. Unexpectedly, even the sequence adjacent to the junction has a significant effect on the crystal assemblies. Six of the immobile junction sequences are completely resistant to crystallization and thus deemed fatal, and molecular dynamics simulations reveal that these junctions invariably lack two discrete ion binding sites that are pivotal for crystal formation. The structures and dynamics detailed here could be used to inform future designs of both crystals and DNA nanostructures more broadly, and have potential implications for the molecular engineering of applied nanoelectronics, nanophotonics, and catalysis within the crystalline context. Engineered crystal architectures from DNA have become a foundational goal for nanotechnological precise arrangement. Here, the authors systematically investigate the structures of 36 immobile Holliday junction sequences and identify the features allowing the crystallisation of most of them, while 6 are considered fatal.

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