Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 25, Issue 27, Pages 18149-18157Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cp01978k
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Nearly half of known proteins have metal co-factors, with evolution selecting multiple metal cations for vital biological processes. Trivalent metal cations, although less prevalent than mono- and divalent counterparts, also play a role. The specific factors governing metal selectivity in trivalent metal centers in proteins are not well understood.
Nearly half of all known proteins contain metal co-factors. In the course of evolution two dozen metal cations (mostly monovalent and divalent species) have been selected to participate in processes of vital importance for living organisms. Trivalent metal cations have also been selected, although to a lesser extent as compared with their mono- and divalent counterparts. Notably, factors governing the metal selectivity in trivalent metal centers in proteins are less well understood than those in the respective divalent metal centers. Thus, the source of high La3+/Ca2+ selectivity in lanthanum-binding proteins, as compared with that of calcium-binding proteins (i.e., calmodulin), is still shrouded in mystery. The well-calibrated thermochemical calculations, performed here, reveal the dominating role of electrostatic interactions in shaping the metal selectivity in La3+-binding centers. The calculations also disclose other (second-order) determinants of metal selectivity in these systems, such as the rigidity and extent of solvent exposure of the binding site. All these factors are also implicated in shaping the metal selectivity in Ca2+-binding proteins.
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