Thermodynamics of the folding of D-glyceraldehyde-3-phosphate dehydrogenase assisted by protein disulfide isomerase studied by microcalorimetry

Eur J Biochem. 2001 Aug;268(15):4183-9. doi: 10.1046/j.1432-1327.2001.02330.x.

Abstract

Thermodynamics of the refolding of denatured D-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) assisted by protein disulfide isomerase (PDI), a molecular chaperone, has been studied by isothermal microcalorimetry at different molar ratios of PDI/GAPDH and temperatures using two thermodynamic models proposed for chaperone-substrate binding and chaperone-assisted substrate folding, respectively. The binding of GAPDH folding intermediates to PDI is driven by a large favorable enthalpy decrease with a large unfavorable entropy reduction, and shows strong enthalpy-entropy compensation and weak temperature dependence of Gibbs free energy change. A large negative heat-capacity change of the binding, -156 kJ.mol(-1).K(-1), at all temperatures examined indicates that hydrophobic interaction is a major force for the binding. The binding stoichiometry shows one dimeric GAPDH intermediate per PDI monomer. The refolding of GAPDH assisted by PDI is a largely exothermic reaction at 15.0-25.0 degrees C. With increasing temperature from 15.0 to 37.0 degrees C, the PDI-assisted reactivation yield of denatured GAPDH upon dilution decreases. At 37.0 degrees C, the spontaneous reactivation, PDI-assisted reactivation and intrinsic molar enthalpy change during the PDI-assisted refolding of GAPDH are not detected.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calorimetry / methods*
  • Cattle
  • Dose-Response Relationship, Drug
  • Entropy
  • Glyceraldehyde-3-Phosphate Dehydrogenases / chemistry*
  • Hot Temperature
  • Kinetics
  • Liver / enzymology
  • Molecular Chaperones / metabolism
  • Protein Disulfide-Isomerases / chemistry*
  • Protein Folding
  • Temperature
  • Thermodynamics
  • Time Factors

Substances

  • Molecular Chaperones
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Protein Disulfide-Isomerases