Thermal stabilty of glucokinase (GK) as influenced by the substrate glucose, an allosteric glucokinase activator drug (GKA) and the osmolytes glycerol and urea

We investigated how glycerol, urea, glucose and a GKA influence kinetics and stability of wild-type and mutant GK. Glycerol and glucose stabilized GK additively. Glycerol barely affected the TF spectra of all GKs but decreased kcat, glucose S0.5 and KD values and ATP KM while leaving cooperativity unchanged. Glycerol sensitized all GKs to GKA as shown by TF. Glucose increased TF of GKs without influence of glycerol on the effect. Glycerol and GKA affected kinetics and binding additively. The activation energies for thermal denaturation of GK were a function of glucose with KDs of 3 and 1 mM without and with glycerol, respectively. High urea denatured wild type GK reversibly at 20 and 60 °C and urea treatment of irreversibly heat denatured GK allowed refolding as demonstrated by TF including glucose response. We concluded: Glycerol stabilizes GK indirectly without changing the folding structure of the apoenzyme, by restructuring the surface water of the protein, whereas glucose stabilizes GK directly by binding to its substrate site and inducing a compact conformation. Glucose or glycerol (alone or combined) is unable to prevent irreversible heat denaturation above 40 °C. However, urea denatures GK reversibly even at 60 °C by binding to the protein backbone and directly interacting with hydrophobic side chains. It prevents irreversible aggregation allowing complete refolding when urea is removed. This study establishes the foundation for exploring numerous instability mutants among the more than 600 variant GKs causing diabetes in animals and humans.

► Structural and functional instability of glucokinase (GK) cause diabetes mellitus. ► Stability and structure of GK are studied by tryptophan fluorescence (TF) and DSC. ► Glucose influences solvent accessibility of GKs 3 tryptophans differentially. ► Glucose and glycerol affect GK kinetics and stability additively. ► Thermal inactivation of GK above 40 °C and reactivation (8 M urea).