In silico study of structural determinants modulating the redox potential of Rigidoporus lignosus and other fungal laccases

J Biomol Struct Dyn. 2012;30(1):89-101. doi: 10.1080/07391102.2012.674275.

Abstract

Laccases are multicopper oxidases in which substrate oxidation takes place at the type-1 (T1) copper site. The redox potential (E (0)) significantly varies amongst members of the family and is a key parameter for substrate specificity. Despite sharing highly conserved features at the T1 copper site, laccases span a large range of E (0), suggesting that the influence of the metal secondary coordination sphere is important. In silico analysis of structural determinants modulating the E (0) of Rigidoporus lignosus and other fungal laccases indicated that different factors can be considered. First, the length of the T1 copper coordinating histidine bond is observed to be longer in high E (0) laccases than in low E (0) ones. The hydrophobic environment around the T1 copper site appeared as another important structural determinant in modulating the E (0), with a stronger hydrophobic environment correlating with higher E (0). The analysis of hydrogen bonding network (HBN) around the T1-binding pocket revealed that the amino acids building up the metal binding site strongly interact with neighbouring residues and contribute to the stabilization of the protein folds. Changes in these HBNs that modified the Cu1 preferred coordination geometry lead to an increase of E (0). The presence of axial ligands modulates the E (0) of T1 to different extent. Stacking interactions between aromatic residues located in the second coordination shell and the metal ion coordination histidine imidazole ring have also been identified as a factor that modulates the E (0). The electrostatic interactions between the T1 copper site and backbone carbonyl oxygen indicate that Cu1-CO=NH distance is longer in the high E (0) laccases. In short, the in silico study reported herein identifies several structural factors that may influence the E (0) of the examined laccases. Some of these are dependent on the nature of the coordination ligands at the T1 site, but others can be ascribed to the hydrophobic effects, HBNs, axial ligations, stacking and electrostatic interactions, not necessary directly interacting with the copper metal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry
  • Binding Sites
  • Fungal Proteins / chemistry*
  • Fungal Proteins / metabolism
  • Fungi / enzymology*
  • Histidine / analogs & derivatives
  • Histidine / chemistry
  • Hydrogen Bonding
  • Laccase / chemistry*
  • Laccase / metabolism
  • Ligands
  • Models, Molecular*
  • Organometallic Compounds / chemistry
  • Oxidation-Reduction
  • Protein Binding
  • Protein Conformation
  • Static Electricity

Substances

  • Amino Acids
  • Fungal Proteins
  • Ligands
  • Organometallic Compounds
  • Histidine
  • copper histidine
  • Laccase