Copper(II), a Peculiar Metal Ion for Complexation With Monensin A Ionophore.
Máté Levente Kis1, Bálint Hajdu1,2, Tamás Jakusch1
1Department of Molecular and Analytical Chemistry, University of Szeged, Szeged, Hungary.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|January 25, 2026
Summary
The antibiotic monensin A forms unique dinuclear copper(II) complexes, unlike other metal ions. These novel coordination compounds are EPR-active, offering new insights into drug-metal interactions.
Area of Science:
- Coordination Chemistry
- Biophysical Chemistry
- Medicinal Chemistry
Background:
- Monensin A is an ionophore that transports sodium ions across cell membranes.
- Monensin A can also bind divalent metal ions, potentially altering its biological activity.
- Previous studies explored monensin A interactions with various metal ions.
Purpose of the Study:
- To investigate the interaction between copper(II) ions and monensin A.
- To characterize the coordination compounds formed between Cu(II) and monensin A.
- To explore the formation of novel dinuclear copper(II) species.
Main Methods:
- Circular dichroism (VIS- and NIR-CD) spectroscopy
- Visible light absorption spectroscopy
- Electron paramagnetic resonance (EPR) spectroscopy
- Electrospray ionization mass spectrometry (ESI-MS)
Main Results:
- Monensin A forms both mono- and bis-Cu(II) complexes.
- Excess Cu(II) salt leads to the formation of previously unobserved dinuclear Cu(II) complexes.
- The dinuclear Cu(II) complex is EPR-active, a rare characteristic for such compounds.
- Counterion origin influences the spectral properties of the dinuclear species.
Conclusions:
- Monensin A forms distinct dinuclear copper(II) complexes.
- These complexes exhibit unique EPR activity.
- Drug-metal ion interactions are significant and should be considered in understanding drug mechanisms.
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