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@ARTICLE{Novak:885886,
      author       = {Novak, Sanja and Zhang, Jing and Kentzinger, Emmanuel and
                      Rücker, Ulrich and Portale, Giuseppe and Jung, Niklas and
                      Jonas, Ulrich and Myung, Jin S. and Winkler, Roland G. and
                      Gompper, Gerhard and Dhont, Jan K. G. and Stiakakis,
                      Emmanuel},
      title        = {{DNA} {S}elf-{A}ssembly {M}ediated by {P}rogrammable
                      {S}oft-{P}atchy {I}nteractions},
      journal      = {ACS nano},
      volume       = {14},
      number       = {10},
      issn         = {1936-086X},
      address      = {Washington, DC},
      publisher    = {Soc.},
      reportid     = {FZJ-2020-04162},
      pages        = {13524–13535},
      year         = {2020},
      abstract     = {Adding shape and interaction anisotropy to a colloidal
                      particle offers exquisitely tunable routes to engineer a
                      rich assortment of complex-architected structures. Inspired
                      by the hierarchical self-assembly concept with block
                      copolymers and DNA liquid crystals and exploiting the unique
                      assembly properties of DNA, we report here the construction
                      and self-assembly of DNA-based soft-patchy anisotropic
                      particles with a high degree of modularity in the system’s
                      design. By programmable positioning of thermoresponsive
                      polymeric patches on the backbone of a stiff DNA duplex with
                      linear and star-shaped architecture, we reversibly drive the
                      DNA from a disordered ensemble to a diverse array of
                      long-range ordered multidimensional nanostructures with
                      tunable lattice spacing, ranging from lamellar to
                      bicontinuous double-gyroid and double-diamond cubic
                      morphologies, through the alteration of temperature. Our
                      results demonstrate that the proposed hierarchical
                      self-assembly strategy can be applied to any kind of DNA
                      nanoarchitecture, highlighting the design principles for
                      integration of self-assembly concepts from the physics of
                      liquid crystals, block copolymers, and patchy colloids into
                      the continuously growing interdisciplinary research field of
                      structural DNA nanotechnology.},
      cin          = {JCNS-2 / PGI-4 / JARA-FIT / IAS-2 / IBI-4 / IBI-5},
      ddc          = {540},
      cid          = {I:(DE-Juel1)JCNS-2-20110106 / I:(DE-Juel1)PGI-4-20110106 /
                      $I:(DE-82)080009_20140620$ / I:(DE-Juel1)IAS-2-20090406 /
                      I:(DE-Juel1)IBI-4-20200312 / I:(DE-Juel1)IBI-5-20200312},
      pnm          = {144 - Controlling Collective States (POF3-144) / 524 -
                      Controlling Collective States (POF3-524) / 6212 - Quantum
                      Condensed Matter: Magnetism, Superconductivity (POF3-621) /
                      6213 - Materials and Processes for Energy and Transport
                      Technologies (POF3-621) / 6G4 - Jülich Centre for Neutron
                      Research (JCNS) (POF3-623) / 551 - Functional Macromolecules
                      and Complexes (POF3-551)},
      pid          = {G:(DE-HGF)POF3-144 / G:(DE-HGF)POF3-524 /
                      G:(DE-HGF)POF3-6212 / G:(DE-HGF)POF3-6213 /
                      G:(DE-HGF)POF3-6G4 / G:(DE-HGF)POF3-551},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {33048544},
      UT           = {WOS:000586793400100},
      doi          = {10.1021/acsnano.0c05536},
      url          = {https://juser.fz-juelich.de/record/885886},
}