Disulfide bridge formation to increase thermostability of DFPase enzyme: A computational study

Comput Biol Chem. 2018 Dec:77:272-278. doi: 10.1016/j.compbiolchem.2018.09.005. Epub 2018 Sep 6.

Abstract

Organophosphate compounds bioremediation by use of organophosphorus degradation enzymes such as DFPase is a developing interest in industry and medicine. The most important problem with the bio-catalytic enzymes is their instability on high temperatures. This work carried out to find suitable locations for introducing disulfide bridges in DFPase enzyme. We employed some computational approaches to design the disulfide bridges and evaluate their roles in the enzyme structural thermostability. According to the in silico results, mutant 6 (V24C, C76) increased the enzyme thermostability relative to wild-type.

Keywords: DFPase; Disulfide bridge; MD simulation; Protein thermostability.

MeSH terms

  • Animals
  • Catalytic Domain
  • Databases, Protein
  • Disulfides / chemistry
  • Enzyme Stability
  • Hot Temperature
  • Loligo / chemistry
  • Loligo / enzymology*
  • Loligo / genetics
  • Molecular Dynamics Simulation
  • Phosphoric Triester Hydrolases / chemistry*
  • Phosphoric Triester Hydrolases / genetics
  • Point Mutation
  • Protein Conformation

Substances

  • Disulfides
  • Phosphoric Triester Hydrolases
  • diisopropyl-fluorophosphatase