Modulation of antioxidant enzyme by light and heavy rare earth metals: A case study with catalase

The present study highlights the hazardous effect of heavy and light rare earth elements (REEs) on bovine liver catalase (BLC) using a combination of spectroscopic and computational methods. The presence of Praseodymium chloride (PrCl<sub>3</sub>) and Gadolinium chloride (GdCl<sub>3</sub>) resulted in a substantial reduction in catalytic efficiency of BLC by approximately 1.8 and 2.6 fold, respectively. The compromised activity was further accompanied by conformational rearrangements at the secondary and tertiary levels as evidenced by circular dichroism (CD) and fluorescence spectroscopy. These analyses revealed a significant decrease in α-helical content and a simultaneous increase in random coils, disrupting intramolecular hydrogen bonding. Furthermore, the zeta potential (ζ) of BLC demonstrated a reversal from negative to positive ζ values upon the addition of PrCl<sub>3</sub> and GdCl<sub>3</sub>, indicating BLC-lanthanide complex formation. Isothermal titration calorimetry (ITC) supports spontaneous interaction with negative free energy favouring endothermic reaction. This was further supported by docking studies which revealed the binding of PrCl<sub>3</sub> and GdCl<sub>3</sub> within the active site of BLC thus interfering with the catalytic ability to degrade hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>). Nevertheless, a significant decline in the melting temperature (T<sub>m</sub>) of BLC was observed in the presence of lanthanides suggesting the thermal instability of the enzyme. Thus, a similar approach could be applied to evaluate the hazardous effects of lanthanides on structural and functional changes in other proteins or similar biomolecules.

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Publication Details

Journal
International Journal of Biological Macromolecules
Published
2024-11-18
DOI
https://doi.org/10.1016/j.ijbiomac.2024.137820
Citations
3
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
Field-Weighted Citation Impact
0.35

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article

Modulation of antioxidant enzyme by light and heavy rare earth metals: A case study with catalase

Umakanta Subudhi, Rashmi Rekha Samal
3 citations
International Journal of Biological Macromolecules
Lanthanide and Transition Metal Complexes
0.35
article

Modulation of antioxidant enzyme by light and heavy rare earth metals: A case study with catalase

Umakanta Subudhi, Rashmi Rekha Samal
article en
3 citations

Abstract

The present study highlights the hazardous effect of heavy and light rare earth elements (REEs) on bovine liver catalase (BLC) using a combination of spectroscopic and computational methods. The presence of Praseodymium chloride (PrCl<sub>3</sub>) and Gadolinium chloride (GdCl<sub>3</sub>) resulted in a substantial reduction in catalytic efficiency of BLC by approximately 1.8 and 2.6 fold, respectively. The compromised activity was further accompanied by conformational rearrangements at the secondary and tertiary levels as evidenced by circular dichroism (CD) and fluorescence spectroscopy. These analyses revealed a significant decrease in α-helical content and a simultaneous increase in random coils, disrupting intramolecular hydrogen bonding. Furthermore, the zeta potential (ζ) of BLC demonstrated a reversal from negative to positive ζ values upon the addition of PrCl<sub>3</sub> and GdCl<sub>3</sub>, indicating BLC-lanthanide complex formation. Isothermal titration calorimetry (ITC) supports spontaneous interaction with negative free energy favouring endothermic reaction. This was further supported by docking studies which revealed the binding of PrCl<sub>3</sub> and GdCl<sub>3</sub> within the active site of BLC thus interfering with the catalytic ability to degrade hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>). Nevertheless, a significant decline in the melting temperature (T<sub>m</sub>) of BLC was observed in the presence of lanthanides suggesting the thermal instability of the enzyme. Thus, a similar approach could be applied to evaluate the hazardous effects of lanthanides on structural and functional changes in other proteins or similar biomolecules.

International Journal of Biological MacromoleculesVol. 283(Pt 3)
Institute of Minerals and Materials Technology (IN), Academy of Scientific and Innovative Research (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Council of Scientific and Industrial Research, India
Openalex Percentile: Top 43%
Lanthanide and Transition Metal Complexes
0.35
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