School of Biomolecular and Biomedical Science, Centre for Synthesis and Chemical Biology, UCD Conway institute, University College Dublin, Belfield, Dublin 4, Ireland.
Protein Sci. 2010 Dec;19(12):2485-97. doi: 10.1002/pro.530.
The conformational change observed upon ligand binding and phosphorylation for the cAMP-dependent protein kinase (protein kinase A-PKA) is of high importance for the regulation of its activity. We calculate pKa values and net charges for 18 3D structures of PKA in various conformations and liganded states to examine the role of electrostatics in ligand binding and activation. We find that the conformational change of PKA takes place without any significant net proton uptake/release at all pH values, thus indicating that PKA has evolved to reduce any pH-dependent barriers to the conformational motion. We furthermore find that the binding of ligands induces large changes in the net charge of PKA at most pH values, but significantly, we find that the net charge difference at physiological pH is close to zero, thus indicating that the active-site pKa values have been preorganized for substrate binding. We are unable to unequivocally resolve the identity of the groups responsible for determining the pH-activity profile of PKA but speculate that the titration of Lys 168 or the titration of ATP itself could be responsible for the loss of activity at high pH values. Finally, we examine the effect of point mutations on the pKa values of the PKA catalytic residues and find these to be relatively insensitive to both noncharge-altering and charge-altering mutations.
配体结合和磷酸化引起的环核苷酸依赖蛋白激酶(蛋白激酶 A-PKA)构象变化对于其活性的调节非常重要。我们计算了 18 种不同构象和配体结合状态下 PKA 的 3D 结构的 pKa 值和净电荷,以研究静电在配体结合和激活中的作用。我们发现,PKA 的构象变化在所有 pH 值下都没有明显的净质子吸收/释放,这表明 PKA 已经进化到减少构象运动的任何 pH 依赖性障碍。此外,我们发现配体的结合在大多数 pH 值下会导致 PKA 的净电荷发生很大变化,但值得注意的是,我们发现生理 pH 值下的净电荷差接近零,这表明活性位点的 pKa 值已经为底物结合进行了预组织。我们无法明确确定决定 PKA pH 活性曲线的基团的身份,但推测 Lys168 的滴定或 ATP 本身的滴定可能是导致高 pH 值下活性丧失的原因。最后,我们研究了点突变对 PKA 催化残基 pKa 值的影响,发现这些残基对非电荷改变和电荷改变突变相对不敏感。