An amphiphilic-DNA platform for the design of crystalline frameworks with programmable structure and functionality
Journal of the American Chemical Society
American Chemical Society (ACS)
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Brady, R., Brooks, N., Fodara, V., Cicuta, P., & Di Michele, L. (2018). An amphiphilic-DNA platform for the design of crystalline frameworks with programmable structure and functionality. Journal of the American Chemical Society https://doi.org/10.1021/jacs.8b09143
The reliable preparation of functional, ordered, nanostructured frameworks would be a game changer for many emerging technologies, from energy storage to nanomedicine. Underpinned by the excellent molecular recognition of nucleic acids, along with their facile synthesis and breadth of available functionalizations, DNA Nanotechnology is widely acknowledged as a prime route for the rational design of nanostructured materials. Yet, the preparation of crystalline DNA frameworks with programmable structure and functionality remains a challenge. Here we demonstrate the potential of simple amphiphilic DNA motifs, dubbed C-stars, as a versatile platform for the design of programmable DNA crystals. In contrast to all-DNA materials, in which structure depends on the precise molecular details of individual build-ing blocks, the self-assembly of C-stars is controlled uniquely by their topology and symmetry. Exploiting this robust self-assembly principle we design a range of topologically identical, but structurally and chemically distinct C-stars that following a one-pot reaction self- assemble into highly porous, functional, crystalline frameworks. Simple design variations allow us to fine-tune the lattice parameter and thus control the partitioning of macromolecules within the frameworks, embed responsive motifs that can induce isothermal disassembly, and include chemical moieties to capture target proteins specifically and reversibly.
LDM, PC and NJB acknowledge support from the EPSRC Programme Grant CAPITALS number EP/J017566/1. LDM acknowledges support from the Leverhulme Trust and the Isaac Newton Trust through an Early Career Fellow- 9 ship (ECF-2015-494) and from the Royal Society through a University Research Fellowship (UF160152). RAB acknowledges support from the EPSRC CDT in Nanoscience and Nanotechnology (NanoDTC), grant number EP/L015978/1.
Leverhulme Trust (ECF-2015-494)
Isaac Newton Trust (MIN 1508(S))
Royal Society (UF160152)
Royal Society (RGF/R1/180043)
EPSRC (via Imperial College London) (CHIS_P39012)
Engineering and Physical Sciences Research Council (EP/L015978/1)
External DOI: https://doi.org/10.1021/jacs.8b09143
This record's URL: https://www.repository.cam.ac.uk/handle/1810/285953