4.8 Article

Site-specific positioning of dendritic alkyl chains on DNA cages enables their geometry-dependent self-assembly

Journal

NATURE CHEMISTRY
Volume 5, Issue 10, Pages 868-875

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEM.1745

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. Centre for Self-Assembled Chemical Structures (CSACS)
  4. Canadian Institute for Advanced Research (CIFAR)
  5. Canadian Institutes of Health Research (CIHR)
  6. NSERC

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Nature uses a combination of non-covalent interactions to create a hierarchy of complex systems from simple building blocks. One example is the selective association of the hydrophobic side chains that are a strong determinant of protein organization. Here, we report a parallel mode of assembly in DNA nanotechnology. Dendritic alkyl-DNA conjugates are hybridized to the edges of a DNA cube. When four amphiphiles are on one face, the hydrophobic residues of two neighbouring cubes engage in an intermolecular 'handshake', resulting in a dimer. When there are eight amphiphiles (four on the top and bottom cube faces, respectively), they engage in an intramolecular 'handshake' inside the cube. This forms the first example of a monodisperse micelle within a DNA nanostructure that encapsulates small molecules and releases them by DNA recognition. Creating a three-dimensional pattern of hydrophobic patches, like side chains in proteins, can result in specific, directed association of hydrophobic domains with orthogonal interactions to DNA base-pairing.

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