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.