Abstract
Here, we introduce a 3D-DNA construction method that assembles a minimum number of DNA strands in quantitative yield, to give a scaffold with a large number of single-stranded arms. This DNA frame is used as a core structure to organize other functional materials in 3D as the shell. We use the ring-opening metathesis polymerization (ROMP) to generate block copolymers that are covalently attached to DNA strands. Site-specific hybridization of these DNA-polymer chains on the single-stranded arms of the 3D-DNA scaffold gives efficient access to DNA-block copolymer cages. These biohybrid cages possess polymer chains that are programmably positioned in three dimensions on a DNA core and display increased nuclease resistance as compared to unfunctionalized DNA cages.
Original language | English |
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Pages (from-to) | 4280-4286 |
Number of pages | 7 |
Journal | Journal of the American Chemical Society |
Volume | 134 |
Issue number | 9 |
DOIs | |
Publication status | Published - 7 Mar 2012 |
Externally published | Yes |