Quest for a stable Cu-ligand complex with a high catalytic activity to produce ROS.
ascorbate
bioinorganic chemistry
copper
dioxygen activation
reactive oxygen species
redox
Journal
Metallomics : integrated biometal science
ISSN: 1756-591X
Titre abrégé: Metallomics
Pays: England
ID NLM: 101478346
Informations de publication
Date de publication:
13 Apr 2024
13 Apr 2024
Historique:
medline:
14
4
2024
pubmed:
14
4
2024
entrez:
13
4
2024
Statut:
aheadofprint
Résumé
Metal ion-catalysed overproduction of reactive oxygen species (ROS) are believed to contribute significantly to oxidative stress and be involved in several biological processes, from immune defence to development of diseases. Among the essential metal ions, copper is one of the most efficient catalysts in ROS production in the presence of O2 and a physiological reducing agent such as ascorbate. To control this chemistry, Cu ions are tightly coordinated to biomolecules. Free or loosely bound Cu ions are generally avoided to prevent their toxicity. In the present report, we aim to find stable Cu-ligand complexes (Cu-L) that can catalyse efficiently the production of ROS in presence of ascorbate under aerobic conditions. Thermodynamic stability would be needed to avoid dissociation in biological environment and high ROS catalysis is of interest for applications as in antimicrobial or anticancer agents. A series of Cu complexes with the well-known tripodal and tetradentate ligands containing a central amine linked to three pyridyl-alkyl arms of different lengths were investigated. The two of them with mixed armlength showed higher catalytic activity in oxidation of ascorbate and subsequent ROS production than Cu salts in buffer, which is an unprecedented result. Despite these high catalytic activities, no increased antimicrobial activity towards E. coli or cytotoxicity against eukaryotic AGS cells in culture related to Cu-L based ROS production could be observed. The potential reasons for discrepancy between in vitro and in cell data will be discussed.
Identifiants
pubmed: 38614957
pii: 7645457
doi: 10.1093/mtomcs/mfae020
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2024. Published by Oxford University Press.