Abstract
The use of three-dimensional self-assembled metallacages (MCgs) as multimodal drug platforms holds great promise. However, the synthesis of MCgs with increased complexity and functionality is a great challenge since understanding of the interaction of MCgs with biological targets is still limited. In this context, this work reports on the integration of a gold(III) porphyrin scaffold into a prismatic MCg structure and explores its application for multimodal therapy of cancer in vitro, namely enabling both photodynamic therapy and chemotherapy. Combining experimental approaches with a state-of-the-art metadynamics theoretical study, we discovered that the gold cage shows unprecedented host-guest interaction- driven selective stabilization of guaninequadruplex (G4) structures - validated anticancer drug targets - disclosing a new mechanism to pursue in the design of supramolecular drugs.
Original language | English |
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Pages (from-to) | 1662-1671 |
Number of pages | 10 |
Journal | CCS Chemistry |
Volume | 6 |
Issue number | 7 |
DOIs | |
State | Published - 1 Jul 2024 |
Keywords
- G4 stabilization
- anticancer agents
- gold metallacages
- host-guest chemistry
- porphyrins