PUBLICATION
Molecular Mechanism of Lead-Induced Superoxide Dismutase Inactivation in Zebrafish Livers
- Authors
- Zhang, H., Liu, Y., Liu, R., Liu, C., Chen, Y.
- ID
- ZDB-PUB-141217-29
- Date
- 2014
- Source
- The journal of physical chemistry. B 118(51): 14820-6 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Calorimetry
- Circular Dichroism
- Female
- Lead/pharmacology*
- Liver/drug effects*
- Liver/enzymology
- Male
- Molecular Docking Simulation
- Spectrophotometry, Ultraviolet
- Superoxide Dismutase/antagonists & inhibitors*
- Zebrafish
- PubMed
- 25494975 Full text @ J. Phys. Chem. B
Citation
Zhang, H., Liu, Y., Liu, R., Liu, C., Chen, Y. (2014) Molecular Mechanism of Lead-Induced Superoxide Dismutase Inactivation in Zebrafish Livers. The journal of physical chemistry. B. 118(51):14820-6.
Abstract
Lead toxicity has been proved to be related with inducing oxidative stress of organisms and causing inactivation of antioxidant enzymes, the mechanism of which remains unknown. This study investigated and compared superoxide dismutase (Cu/Zn SOD) activity inhibited in lead-treated zebrafish livers and explored the mechanism of SOD inactivation by lead at the molecular level using multiple spectroscopic techniques, isothermal titration calorimetric (ITC) measurement, molecular docking study and ICP-AES detection. Results showed lead exposure decreased SOD activities in zebrafish livers due to direct interactions between lead and SOD, resulting in conformational and functional changes of the enzyme. To be specific, Studies at the molecular level indicated that lead bound into the active site channel of SOD, hindered the path of the catalytic substrate (O2(-•)), damaged its skeleton conformation and secondary structure, and interacted with the enzymatically related residue (Arg 141) through electrostatic forces (ΔH < 0, ΔS > 0), and caused the release of Cu(2+) and Zn(2+) from the catalytic pocket of SOD. This work shows a correlation between results on organismal and molecular levels, and obtains a possible model hypothesizing mechanisms of lead toxicity using in vitro experiments instead of in vivo ones.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping