1. Modeling of laccase inhibition by formetanate pesticide using theoretical approaches
- Author
-
Ana Caroline V. Martins, Geancarlo Zanatta, Francisco W.P. Ribeiro, Adriana N. Correia, Simone Morais, Pedro de Lima-Neto, Valder N. Freire, and Repositório Científico do Instituto Politécnico do Porto
- Subjects
Models, Molecular ,Immobilized enzyme ,Protein Conformation ,Static Electricity ,Biophysics ,Amino acid residues ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Enzyme catalysis ,Enzymatic catalysis ,chemistry.chemical_compound ,Electrochemistry ,Moiety ,Organic chemistry ,Quantum chemical calculations ,Enzyme Inhibitors ,Pesticides ,Physical and Theoretical Chemistry ,Inhibition ,Trametes ,Laccase ,Dose-Response Relationship, Drug ,Chemistry ,Electric Conductivity ,General Medicine ,Enzymes, Immobilized ,021001 nanoscience & nanotechnology ,Combinatorial chemistry ,0104 chemical sciences ,Colloidal gold ,Formetanate ,Molecular docking ,Biocatalysis ,Density functional theory ,Quantum Theory ,Environmental Pollutants ,Carbamates ,Gold ,Cyclic voltammetry ,0210 nano-technology ,Biosensor - Abstract
The inhibition of laccase enzymatic catalytic activity by formetanate hydrochloride (FMT) was investigated by cyclic voltammetry and by quantum chemical calculations based on density functional theory with a protein fragmentation approach. The cyclic voltammograms were obtained using a biosensor prepared by enzyme immobilization on gold electrodes modified with gold nanoparticles and 4-aminophenol as the target molecule. The decrease in the peak current in the presence of FMT was used to characterize the inhibition process. The calculations identified Asp206 as the most relevant moiety in the interaction of FMT with the laccase enzymatic ligand binding domain. The amino acid residue Cys453 was important, because the Cys453-FMT interaction energy was not affected by the dielectric constant, although it was not a very close residue. This study provides an overview of how FMT inhibits laccase catalytic activity.
- Published
- 2016