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作 者:Tamara Rodríguez-Prieto Darren Wragg Nicole Heiduk Mihyun Park Nicole Strittmatter Roland A.Fischer Angela Casini Guillermo Moreno-Alcántar
机构地区:[1]Chair of Medicinal and Bioinorganic Chemistry,Department of Chemistry,School of Natural Sciences,Technical University of Munich,85748 Garching b.München [2]Professorship for Analytical Chemistry,Department of Chemistry,School of Natural Sciences,Technical University of Munich,85748 Garching b.München [3]Chair of Inorganic and MetalOrganic Chemistry,Department of Chemistry,School of Natural Sciences,Technical University of Munich,85748 Garching b.München [4]Munich Data Science Institute(MDSI),Technical University of Munich,85748 Garching b.München
出 处:《CCS Chemistry》2024年第7期1662-1671,共10页中国化学会会刊(英文)
摘 要: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 guanine-quadruplex(G4)structures-validated anticancer drug targets-disclosing a new mechanism to pursue in the design of supramolecular drugs.
关 键 词:gold metallacages PORPHYRINS G4stabili-zation host-guestchemistry anticanceragents
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