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. 2001 Mar 1;117(3):275–286. doi: 10.1085/jgp.117.3.275

Table 2.

The Effects of Extracellular [Na+] on Mg2+ Dissociation and Permeation

k0 −Mg ɛ k0 pMg λ
s−1 s−1
[Na+]ex = 25 mM 6,909 ± 1,888 0.36 ± 0.08 675 ± 288 0.03 ± 0.03
[Na+]ex = 50 mM 5,860 ± 1,259 671 ± 283
[Na+]ex = 100 mM 4,417 ± 760 650 ± 262
[Na+]ex = 150 mM 3,513 ± 480 645 ± 249

k0 −Mg is the rate constant for Mg2+ dissociation from the pore to the extracellular solution, and k0 pMg is the rate constant for Mg2+ permeation into the intracellular solution in the absence of a membrane potential. The dissociation rate constant decreases as extracellular [Na+] increases because a bound Mg2+ cannot return to the extracellular solution when Na+ occupies an external binding site. ɛ is the electrical distance from the Mg2+ binding site to peak of the dissociation barrier, and is λ the electrical distance to the peak of the permeation barrier (see Fig. 6). We assume that these values do not change with the extracellular [Na+]. The values (±SD) were obtained by fitting globally (i.e., simultaneously to multiple data sets) to the data shown in Fig. 5 B.