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DNA damage induced by a chromium(III) Schiff base complex is reversible under physiological condition
V G Vaidyanathan1, T Weyhermuller, Balachandran Unni Nair
1Central Leather Research Institute, Adyar, Chennai 600 020, India.
Journal of Inorganic Biochemistry
|October 6, 2005
Summary
This study characterizes a chromium(III) complex, [Cr(naphen)(H2O)(2)]+, which binds to DNA and promotes its cleavage. DNA damage induced by this complex can be repaired by bacterial enzymes.
Area of Science:
- Bioinorganic Chemistry
- Coordination Chemistry
- Molecular Biology
Background:
- The development of metal complexes for DNA interaction is crucial for therapeutic applications.
- Chromium complexes, particularly those with salen-type ligands, show potential for DNA binding and cleavage activities.
Purpose of the Study:
- To structurally characterize the novel chromium(III) complex, [Cr(naphen)(H2O)(2)]+.
- To investigate the DNA binding and cleavage mechanisms of the complex.
- To assess the repairability of DNA damage induced by the complex.
Main Methods:
- X-ray crystallography for structural characterization.
- DNA binding studies using techniques like UV-Vis spectroscopy and fluorescence.
- DNA cleavage assays in the presence of biological reductants and oxidants.
- Electron Paramagnetic Resonance (EPR) spectroscopy to identify reactive oxygen species.
- Cell viability assays with Escherichia coli DNA repair enzymes.
Main Results:
- The chromium(III) complex [Cr(naphen)(H2O)(2)]+ was structurally characterized, revealing an extended aromatic system.
- The complex binds intercalatively to calf thymus DNA (CT DNA).
- It promotes DNA cleavage via hydroxyl radical generation in the presence of ascorbate and hydrogen peroxide.
- DNA damage induced by the complex is repairable by Escherichia coli DNA repair enzymes.
Conclusions:
- The [Cr(naphen)(H2O)(2)]+ complex exhibits DNA binding and cleavage properties.
- Hydroxyl radicals are implicated in the oxidative DNA cleavage mechanism.
- The study demonstrates the potential for DNA repair of the induced damage, suggesting therapeutic relevance.