4.8 Article

One-Pot Assembly of a Hetero-dimeric DNA Origami from Chip-Derived Staples and Double-Stranded Scaffold

Journal

ACS NANO
Volume 7, Issue 2, Pages 903-910

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn302322j

Keywords

structural DNA nanotechnology; molecular self-assembly; DNA origami; chip-synthesized oligonucleotides; synthetic biology; gene-synthesis; inkjet

Funding

  1. [NSF-EMT-0829749]
  2. [NSF-CCF-0835794]
  3. [NSF-IRES-0965965]
  4. [ONR-N000140910249]
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [0835794] Funding Source: National Science Foundation
  7. Office Of The Director
  8. Office Of Internatl Science &Engineering [1246799] Funding Source: National Science Foundation

Ask authors/readers for more resources

Although structural DNA nanotechnology, and especially scaffolded DNA origami, hold great promise for bottom-up fabrication of novel nanoscale materials and devices, concerns about scalability have tempered widespread enthusiasm. Here we report a single-pot reaction where both strands of double-stranded M13-bacteriophage DNA are simultaneously folded into two distinct shapes that then heterodimerize with high yield. The fully addressable, two-dimensional heterodimer DNA origami, with twice the surface area of standard M13 origami, formed in high yield (81% of the well-formed monomers undergo dimerization). We also report the concurrent production of entire sets of staple strands by a unique, nicking strand-displacement amplification (nSDA) involving reusable surface-bound template strands that were synthesized in situ using a custom piezoelectric inkjet system. The combination of chip-based staple strand production, double-sized origami, and high-yield one-pot assembly markedly increases the useful scale of DNA origami.

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