Residues contributing to the Ca2+ and K+ binding pocket of the NCKX2 Na+/Ca2+-K+ exchanger

The Na+/Ca2+-K+ exchanger (NCKX) extrudes Ca2+ from cells utilizing both the inward Na+ gradient and the outward K+ gradient. NCKX is thought to operate by a consecutive mechanism in which a cation binding pocket accommodates both Ca2+ and K+ and alternates between inward and outward facing conformations. Here we developed a simple fluorometric method to analyze changes in K+ and Ca2+ dependences of mutant NCKX2 proteins in which candidate residues within membrane-spanning domains were substituted. The largest shifts in both K+ and Ca2+ dependences compared with wild-type NCKX2 were observed for the charge-conservative substitutions of Glu(188) and Asp(548), whereas the size-conservative substitutions resulted in nonfunctional proteins. Substitution of several other residues including two proline residues (Pro(187) and Pro(547)), three additional acidic residues (Asp(258), Glu(265), Glu(533)), and two hydroxyl-containing residues (Ser(185) and Ser(545)) showed smaller shifts, but shifts in Ca2+ dependence were invariably accompanied by shifts in K+ dependence. We conclude that Glu(188) and Asp(548) are the central residues of a single cation binding pocket that can accommodate both K+ and Ca2+. Furthermore, a single set of residues lines a transport pathway for both K+ and Ca2+.