RESUMEN
A novel DNA-microgel hybrid system with dual thermal responsiveness is introduced uitilizing covalent coupling of single stranded DNA (ssDNA) to thermoresponsive microgels (µGs). The spatial distribution of the coupling sites for the ssDNA was characterized with 3D superresolution fluorescence microscopy. The DNA-functionalized µGs remain thermoresponsive and can take up dye-labeled complementary ssDNA, which can be released again by overcoming the dehybridization temperature of the DNA independently of the volume phase transition (VPT) of the µGs. The same holds for nano-objects represented by plasmonic gold nanoparticles (AuNPs), the penetration depth of which was visualized via TEM tomography and 3D reconstruction and which show enhanced plasmonic coupling in the collapsed state of the µG and thus gets switchable. In contrast, if ssDNA was taken up just by non-specific interactions, i.e. into non-functionalized µGs, its release is temperature-independent and can only be induced by increasing the salt concentration. Thus, the incorporated ssDNA represents highly selectice binding sites determined by their base number and sequence, which makes the VPT, beeing determined by the µG composition, and the reversible uptake and release enabled through programmable DNA hybridization are independent features. The combination with the typically high biocompatibility and the retained swellability and permeability hold promise for new fundamental insights as well as for potential applications in biological environments.