Urea-induced denaturation of human calcium/calmodulin-dependent protein kinase IV: a combined spectroscopic and MD simulation studies

Calcium/calmodulin-dependent protein kinase IV (CaMKIV) is a multifunctional enzyme which belongs to the Ser/Thr kinase family. CaMKIV plays important role in varieties of biological processes such as gene expression regulation, memory consolidation, bone growth, T-cell maturation, sperm motility, regulation of microtubule dynamics, cell-cycle progression, and apoptosis. To measure stability parameters, urea-induced denaturation of CaMKIV was carried out at pH 7.4 and 25°C, using three different probes, namely far-UV CD, near-UV absorption, and tryptophan fluorescence. A coincidence of normalized denaturation curves of these optical properties suggests that urea-induced denaturation is a two-state process. Analysis of these denaturation curves gave values of 4.20 ± 0.12 kcal mol⁻¹, 2.95 ± 0.15 M, and 1.42 ± 0.06 kcal mol⁻¹ M⁻¹ for (Gibbs free energy change (Δ<i>G</i>_D) in the absence of urea), <i>C</i>_m (molar urea concentration ([urea]) at the midpoint of the denaturation curve), and <i>m</i> (=∂Δ<i>G</i>_D/∂[urea]), respectively. All these experimental observations have been fully supported by 30 ns molecular dynamics simulation studies.