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Thermo-Programmed Synthetic DNA-Based Receptors.

Davide MariottiniAndrea IdiliGianfranco ErcolaniFrancesco Ricci
Published in: ACS nano (2023)
Herein, we present a generalizable and versatile strategy to engineer synthetic DNA ligand-binding devices that can be programmed to load and release a specific ligand at a defined temperature. We do so by re-engineering two model DNA-based receptors: a triplex-forming bivalent DNA-based receptor that recognizes a specific DNA sequence and an ATP-binding aptamer. The temperature at which these receptors load/release their ligands can be finely modulated by controlling the entropy associated with the linker connecting the two ligand-binding domains. The availability of a set of receptors with tunable and reversible temperature dependence allows achieving complex load/release behavior such as sustained ligand release over a wide temperature range. Similar programmable thermo-responsive synthetic ligand-binding devices can be of utility in applications such as drug delivery and production of smart materials.
Keyphrases
  • circulating tumor
  • cell free
  • single molecule
  • drug delivery
  • nucleic acid
  • circulating tumor cells
  • cancer therapy
  • sensitive detection