Molecular determinants of the inhibition of human Kv1.5 potassium currents by external protons and Zn(2+)

doi:10.1113/jphysiol.2001.014456

. 2002 May 15;541(Pt 1):9-24.

doi: 10.1113/jphysiol.2001.014456.

Molecular determinants of the inhibition of human Kv1.5 potassium currents by external protons and Zn(2+)

Steven J Kehl¹, Cyrus Eduljee, Daniel C H Kwan, Shetuan Zhang, David Fedida

Affiliations

PMID: 12015417
PMCID: PMC2290311
DOI: 10.1113/jphysiol.2001.014456

Molecular determinants of the inhibition of human Kv1.5 potassium currents by external protons and Zn(2+)

Steven J Kehl et al. J Physiol. 2002.

. 2002 May 15;541(Pt 1):9-24.

doi: 10.1113/jphysiol.2001.014456.

Authors

Steven J Kehl¹, Cyrus Eduljee, Daniel C H Kwan, Shetuan Zhang, David Fedida

Affiliation

¹ Department of Physiology, University of British Columbia, 2146 Health Sciences Mall, Vancouver, British Columbia, Canada V6T 1Z3. skehl@interchange.ubc.ca

PMID: 12015417
PMCID: PMC2290311
DOI: 10.1113/jphysiol.2001.014456

Abstract

Using human Kv1.5 channels expressed in HEK293 cells we assessed the ability of H+o to mimic the previously reported action of Zn(2+) to inhibit macroscopic hKv1.5 currents, and using site-directed mutagenesis, we addressed the mechanistic basis for the inhibitory effects of H(+)(o) and Zn(2+). As with Zn(2+), H(+)(o) caused a concentration-dependent, K(+)(o)-sensitive and reversible reduction of the maximum conductance (g(max)). With zero, 5 and 140 mM K(+)(o) the pK(H) for this decrease of g(max) was 6.8, 6.2 and 6.0, respectively. The concentration dependence of the block relief caused by increasing [K(+)](o) was well fitted by a non-competitive interaction between H(+)(o) and K(+)(o), for which the K(D) for the K(+) binding site was 0.5-1.0 mM. Additionally, gating current analysis in the non-conducting mutant hKv1.5 W472F showed that changing from pH 7.4 to pH 5.4 did not affect Q(max) and that charge immobilization, presumed to be due to C-type inactivation, was preserved at pH 5.4. Inhibition of hKv1.5 currents by H+o or Zn(2+) was substantially reduced by a mutation either in the channel turret (H463Q) or near the pore mouth (R487V). In light of the requirement for R487, the homologue of Shaker T449, as well as the block-relieving action of K(+)(o), we propose that H(+) or Zn(2+) binding to histidine residues in the pore turret stabilizes a channel conformation that is most likely an inactivated state.

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Figures

**Figure 1. Extracellular acidification decreases the maximum conductance (g_max) and causes a rightward shift of the conductance-voltage (g(V)) relationship for hKv1.5 currents**
Panels A and B show, respectively, representative control (pH 7.4) and treated (pH 6.4) currents evoked by the voltage protocol shown above each family of traces. Successive pulse command voltages were incremented by 5 mV but for clarity only alternate traces are shown. The change of the range of pulse voltages at pH 6.4 was necessary to compensate for the gating shift. The holding potential in this and other figures was −80 mV, except where noted. Inset traces show the tail currents at a higher gain. Tail current amplitudes, obtained by extrapolating the fit of a single exponential function to the start of the step to −50 mV, are plotted in C and fitted to a Boltzmann function to obtain the equivalent of the g(V) relationship. Acidification shifted the V_1/2 from −6.2 mV to 4.3 mV and the maximum current decreased from 1.7 nA to 0.24 nA, which corresponds to a g_max relative to that at pH 7.4 (relative g_max) of 0.14.

**Figure 9. The effect of the stimulus frequency and holding potential on the inhibition of wild-type hKv1.5 currents by Ho+**
This graph, which is representative of the results obtained from six such experiments, three at pH 5.9 and three with 1 mm Zn²⁺, plots the amplitude of tail currents measured at −50 mV following a 300 ms step to 60 mV to maximally activate channels. After 10 consecutive control responses in standard external saline (pH 7.4, 3.5 mm $K_{o}^{+}$ ) and evoked at 5 s intervals from a holding potential of −80 mV, pulsing was stopped and 5 ml of test solution was perfused to change the extracellular pH to 5.9 for the duration indicated by arrows. Resumption of the step commands approximately 2 min after extracellular acidification showed an immediate ≈75 % reduction of the tail current amplitude. The identical effect was obtained for each of two subsequent pulse trains confirming that the inhibition was not affected by a period without stimulation. Changing the holding potential to −100 mV also had no effect on the current amplitude. Returning to pH 7.4 medium while pulsing shows the effect rapidly (within 15 s) and completely reverses, implying that a change of the internal pH is not involved.

**Figure 2. Increasing Ko+ reduces the inhibition of hKv1.5 current by protons**
Traces obtained from three different cells showing the current at pH 7.4 (control, top row) and pH 6.4 (treated, lower row) in, from left to right, zero, 3.5 and 140 mm $K_{o}^{+}$ . In zero $K_{o}^{+}$ , control and treated pulse currents were evoked by 300 ms pulses from −50 to 45 mV in 5 mV steps; in 3.5 mm $K_{o}^{+}$ , the pulse command range was −50 to 45 mV at pH 7.4 and −30 to 65 mV at pH 6.4; in 140 mm $K_{o}^{+}$ , the range for pulse voltages was −40 to 55 mV. For clarity, only alternate current traces are shown. The corresponding control (○) and treated g(V) relationships, obtained from a number of similar experiments, are shown in the graph at the bottom of each column. Treated data were normalized with respect both to the g_max at pH 6.4 (▪) and to the control g_max (•). The relative g_max at pH 6.4 in zero, 3.5 and 140 mm $K_{o}^{+}$ was 0.19 ± 0.02 (n = 12), 0.56 ± 0.01 (n = 6), and 0.81 ± 0.12 (n = 6), respectively. In zero $K_{o}^{+}$ , V_1/2 and s changed from −21.4 ± 4.3 and 4.7 ± 0.5 mV at pH 7.4 to −8.2 ± 4.0 and 7.1 ± 0.3 mV at pH 6.4, respectively. In 3.5 mm $K_{o}^{+}$ , the corresponding values were −18.3 ± 1.9 mV and 3.9 ± 0.4 mV at pH 7.4 and −10.5 ± 1.2 mV and 3.9 ± 0.4 mV at pH 6.4; and, in 140 mm $K_{o}^{+}$ , −26.2 ± 1.1 mV and 3.8 ± 0.3 mV at pH 7.4 and −12.3 ± 1.1 mV and 3.8 ± 0.4 mV at pH 6.4.

**Figure 3. The concentration dependence of the inhibition of Kv1.5 currents by protons in zero (•), 5 (▪) and 140 mm (▴) Ko+**
Data for zero $K_{o}^{+}$ were obtained with either 143.5 mm Na⁺ (•) or 143.5 mm NMG⁺ (○) as the major extracellular cation. The lines represent the best fit to eqn (3). The fitted values for the equilibrium dissociation constant for protons (K_H), the pK_H and n_H were, in zero $K_{o}^{+}$ and 143.5 mm NMG⁺: 128 ± 53 nm (mean ± s.d.), 6.9 and 1.2 ± 0.5; in zero $K_{o}^{+}$ and 143.5 mm Na⁺: 153 ± 13 nm, 6.8 and 1.5 ± 0.2; in 5 mm $K_{o}^{+}$ : 590 ± 85 nm, 6.2 and 1.6 ± 0.4; and in 140 mm $K_{o}^{+}$ : 1.1 ± 0.11 μM, 6.0 and 1.8 ± 0.3. Although the pK_H estimates with either Na⁺ or NMG⁺ as the extracellular cation are similar, the increase of the relative g_max with NMG⁺ at pH 8.4 was significantly greater. Consistent with a non-competitive *versus* competitive interaction between $H_{o}^{+}$ and $K_{o}^{+}$ (see Fig. 4), the increase of K_H going from zero to 5 mm $K_{o}^{+}$ was greater than that going from 5 mm to 140 mm.

**Figure 4. The concentration dependence of the antagonism by Ko+ and Cso+ of the inhibition of hKv1.5 currents by Ho+**
The relative g_max at different $K_{o}^{+}$ concentrations is plotted for pH 6.9 (▪), pH 6.4 (▴) and pH 5.9 (•). The data for pH 6.9 and 5.4 were obtained with zero, 5, 20 and 140 mm $K_{o}^{+}$ . At pH 6.4, $K_{o}^{+}$ was zero, 1, 3.5, 5, 10, 20, 80 and 140 mm. Assessment of the block-relieving effect of ${Cs}_{o}^{+}$ (▿) was done with concentrations of 3.5, 20 and 140 mm. The lines represent the best fit of the data to eqn (4) (see Methods). With the values for K_H and n_H fixed to those obtained directly from the data in Fig. 3 (153 nm and 1.5, respectively) the best-fit values for K_K and α were 0.65 ± 0.27 mm and 5.5 ± 0.7. ${Cs}_{o}^{+}$ appears to be equivalent to $K_{o}^{+}$ in its antagonism of the proton block. The best fit of the data at pH 6.9 was obtained with 0.93 ± 2.8 mm for K_K and 6.2 ± 9.1 for α; at pH 5.9 the corresponding values were 0.66 ± 0.48 mm and 6.2 ± 1. These estimates for K_K are very near those estimated for the $K_{o}^{+}$ relief of the Zn²⁺ block (≈0.5 mm; Zhang *et al.* 2001b).

**Figure 5. The structure of the S5, S6 and the pore (P) loop of Kv1.5 inferred from the crystal structure of KcsA**
A, the sequence alignment for Kv1.5, *Shaker* and KcsA between the turret and the outer pore mouth. B, a side view of the KcsA channel in which the foreground and background α-subunits have been removed for clarity. The α-subunit of voltage-gated K⁺ channels has an additional four transmembrane segments (S1-S4) that are not illustrated. Sites at which mutations were made, namely H463 and R487, are shown at their homologous positions in the KcsA crystal structure. The orientation of the side chains of these two residues is tentative.

**Figure 6. A point mutation in the turret (S5-P loop), H463Q, reduces the inhibition but not the gating shift caused by Ho+ and Zn²⁺**
A, the g(V) relationship in zero $K_{o}^{+}$ at pH 8.4 (♦), pH 7.4 (○), pH 6.4 (▪), pH 5.9 (▴) and pH 5.5 (▾) after normalization with respect to the g_max at pH 7.4. Values for the relative g_max, V_1/2 and s were: at pH 8.4, 1.1 ± 0.02, −23.9 ± 1.3 mV and 5.4 ± 0.5 mV (n = 5); at pH 7.4, 1, −20.1 ± 1.0 mV and 4.6 ± 0.2 mV(n = 28); at pH 6.4, 1.06 ± 0.03, −13.0 ± 0.5 mV and 4.0 ± 0.5 mV (n = 3); at pH 5.9, 0.86 ± 0.08, 7.6 ± 0.7 mV and 5.6 ± 0.4 mV (n = 8); and, at pH 5.5, 0.63 ± 0.04, 19.2 ± 1.7 mV and 5.7 ± 0.4 mV (n = 7). B, the concentration dependence of the reduction of g_max by protons. Fitting of the data to the Hill equation gave a K_D of 4.7 ± 1.9 μM (pK_H ≈ 5.3) and n_H of 1.0 ± 0.4. The g_max- $H_{o}^{+}$ concentration relationship for wild-type hKv1.5 is represented by the dashed line. C, the g(V) relationship as described for A but with zero (○), 50 μM (□), 200 μM(▾), 1 mm (▪) and 2.5 mm (▴) of Zn²⁺. The relative g_max, V_1/2, and s were 1, −14.9 ± 0.9 mV and 4.8 ± 0.3 mV for the control (n = 27); 0.87 ± 0.08, −1.9 ± 0.9 mV and 6.2 ± 0.9 mV for 50 μM Zn²⁺ (n = 5); 0.77 ± 0.09, 7.1 ± 1.1 mV and 5.9 ± 0.2 mV for 200 μM Zn²⁺ (n = 6); 0.47 ± 0.04, 18.5 ± 2.0 mV and 6.0 ± 0.7 mV for 1 mm Zn²⁺ (n = 10); and 0.52 ± 0.009, 27.2 ± 2.3 mV and 6.4 ± 0.8 mV for 2.5 mm Zn²⁺ (n = 5). D, as described for B but with Zn²⁺. The best-fit values for K_Zn and n_H were 1.7 ± 1 mm and 0.5 ± 0.2. The dashed line indicates the concentration-response relationship for wild-type Kv1.5 in zero $K_{o}^{+}$ (K_Zn = 69 μM, n_H = 0.9; Zhang *et al.* 2001b).

**Figure 7. In hKv1.5 H463G slow inactivation is greatly accelerated and the conductance collapses in zero Ko+ at pH 7.4**
A, shown for comparison are the currents from hKv1.5 H463Q evoked in zero $K_{o}^{+}$ by 300 ms pulses to between −40 and 40 mV in 10 mV increments. B, hKv1.5 H463G currents recorded using the same stimulus protocol but with 3.5 mm $K_{o}^{+}$ . The solid line superimposed on the current at 40 mV represents the best fit of the current decay to a single exponential function. The mean time constant for inactivation at 40 mV was 73 ± 8 ms (n = 4). C, from the same cell as in B and using the same voltage command protocol after switching to zero $K_{o}^{+}$ at pH 7.4. Unlike either wild-type Kv1.5 H463 (Fig. 1) or Kv1.5 H463Q, $K_{o}^{+}$ is required for hKv1.5 H463G channels to function normally at pH 7.4. Complete recovery was obtained after returning to K⁺-containing bath solution (not shown).

**Figure 8. A mutation near the pore mouth, R487V, substantially reduces the sensitivity to inhibition by Ho+ and Zn²⁺**
A, the g(V) relationship in zero $K_{o}^{+}$ at pH 8.4 (♦), pH 7.4 (○), pH 6.4 (▪), pH 5.9 (▴) and pH 5.5 (▾) after normalization with respect to g_max at pH 7.4. The values for the relative g_max, V_1/2 and s were, respectively, 1.04 ± 0.02, −28.5 ± 1.1 mV, 4.6 ± 1.0 mV at pH 8.4 (n = 3); 1, −18.1 ± 0.9 mV, 4.5 ± 0.2 mV at pH 7.4 (n = 17); 1.04 ± 0.06, −1.8 ± 1.3 mV, 5.6 ± 0.4 mV at pH 6.4 (n = 5); 0.92 ± 0.03, 6.4 ± 1.3, 4.9 ± 0.4 at pH 5.9; and 0.87 ± 0.03, 15.5 ± 1.6 mV, 5.5 ± 0.2 mV at pH 5.5 (n = 5). B, the concentration-response relationship for the reduction of g_max by protons. The continuous line, representing the best fit of the data to the Hill equation, was obtained with K_H = 23 μM (pK_H of 4.6) and n_H = 0.8. C, the g(V) relationship in zero $K_{o}^{+}$ and with Zn²⁺ concentrations of 10 μM (•), 25 μM (♦), 100 μM (⋄), 200 μM (▾), 1 mm (▪) and 2.5 mm (▴) after normalization with respect to the control (○) g_max. The relative g_max, V_1/2 and s were, respectively, 1, −13.4 ± 1.5 mV, 4.5 ± 0.3 mV for the control (n = 15), 0.99 ± 0.01, −5.9 ± 1.5 mV, 5.4 ± 0.4 mV in 10 μM Zn²⁺ (n = 4); 0.92 ± 0.05, −5.7 ± 0.1 mV, 4.7 ± 0.5 mV in 25 μM Zn²⁺ (n = 3); 0.80 ± 0.02, 2.8 ± 1.8 mV, 4.8 ± 0.5 mV in 100 μM Zn²⁺ (n = 4); 0.78 ± 0.02, 5.2 ± 1.6 mV, 5.3 ± 0.3 mV in 200 μM Zn²⁺ (n = 5); 0.70 ± 0.05, 21.0 ± 1.2 mV, 5.9 ± 0.3 mV in 1 mm Zn²⁺ (n = 3); and 0.59 ± 0.02, 28.9 ± 1.1 mV, 5.9 ± 0.3 mV in 2.5 mm Zn²⁺ (n = 5). D, as described for B but with Zn²⁺. The continuous line represents the best fit of the hKv1.5 R487V data to the sum of two Hill equations. Binding at the higher affinity site (K_Zn = 29 ± 0.2 μM) accounted for ≈20 % of the inhibition. The apparent elimination of the higher affinity site in the double mutant Kv1.5 R487V, H463Q (▵ and dashed line) suggests that it may reflect Zn²⁺ binding to H463. The extrapolated K_Zn for the lower affinity site in the R487V mutant was 6.4 ± 0.07 mm. Again, the dotted lines in B and D represent the corresponding concentration-response curves for wild-type hKv1.5 (Zhang *et al.* 2001b).

**Figure 10. Extracellular acidification to pH 5.4 causes a depolarizing shift of the Q_on(V) and Q_off(V) relationships but does not reduce Q_max**
Panels A and B show at pH 7.4 and 5.4, respectively, the on- and off-gating currents recorded when the membrane was depolarized for 12 ms from a holding potential of −100 mV to between −60 and 100 mV (A) or −60 and 150 mV (B) in 10 mV increments before stepping back to −100 mV. Outward charge movement (Q_on) induced by the depolarization was determined by integrating the on-gating currents at pH 7.4 (○) and 5.4 (•), and is plotted in panel E. For the Q_on(V) relationship in E, the fitted values for V_1/2 and s were, respectively, −2.2 mV and 6.5 mV at pH 7.4 and 50.2 mV and 11.8 mV at pH 5.4. Q_max was not significantly affected by extracellular acidification. C and D, from the same cell as in A and B, these panels show the off-gating currents following a 12 ms step from −80 mV to 50 mV in pH 7.4 (C) or to 100 mV at pH 5.4 (D) to move Q_max. Off-gating current was recorded in 10 mV increments between −200 and −10 mV at pH 7.4 and between −200 and 40 mV at pH 5.4. Charge return at pH 7.4 (▵) and pH 5.4 (▴) is plotted against the repolarization voltage in E to obtain the Q_off(V) relationship. Extracellular acidification changed the V_1/2 of Q_off(V) from −100.5 mV to −72.9 mV and s increased from 9.4 mV to 13.1 mV. Both at pH 7.4 and pH 5.4 there is a leftward shift of the voltage dependence of Q_off relative to Q_on(*V).*

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References

1. Aiyar J, Withka JM, Rizzi JP, Singleton DH, Andrews GC, Lin W, Boyd J, Hanson DC, Simon M, Dethlefs B. Topology of the pore-region of a K+ channel revealed by the NMR-derived structures of scorpion toxins. Neuron. 1995;15:1169–1181. - PubMed
1. Backx PH, Yue DT, Lawrence JH, Marban E, Tomaselli GF. Molecular localization of an ion-binding site within the pore of mammalian sodium channels. Science. 1992;257:248–251. - PubMed
1. Baukrowitz T, Yellen G. Modulation of K+ current by frequency and external [K+]: A tale of two inactivation mechanisms. Neuron. 1995;15:951–960. - PubMed
1. Baukrowitz T, Yellen G. Two functionally distinct subsites for the binding of internal blockers to the pore of voltage-activated K+ channels. Proceedings of the National Academy of Sciences of the USA. 1996;93:13 357–13 361. - PMC - PubMed
1. Blaustein RO, Cole PA, Williams C, Miller C. Tethered blockers as molecular ‘tape measures’ for a voltage-gated K+ channel. Nature Structural Biology. 2000;7:309–311. - PubMed

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[1] Aiyar J, Withka JM, Rizzi JP, Singleton DH, Andrews GC, Lin W, Boyd J, Hanson DC, Simon M, Dethlefs B. Topology of the pore-region of a K+ channel revealed by the NMR-derived structures of scorpion toxins. Neuron. 1995;15:1169–1181. - PubMed

[2] Aiyar J, Withka JM, Rizzi JP, Singleton DH, Andrews GC, Lin W, Boyd J, Hanson DC, Simon M, Dethlefs B. Topology of the pore-region of a K+ channel revealed by the NMR-derived structures of scorpion toxins. Neuron. 1995;15:1169–1181. - PubMed

[3] Backx PH, Yue DT, Lawrence JH, Marban E, Tomaselli GF. Molecular localization of an ion-binding site within the pore of mammalian sodium channels. Science. 1992;257:248–251. - PubMed

[4] Backx PH, Yue DT, Lawrence JH, Marban E, Tomaselli GF. Molecular localization of an ion-binding site within the pore of mammalian sodium channels. Science. 1992;257:248–251. - PubMed

[5] Baukrowitz T, Yellen G. Modulation of K+ current by frequency and external [K+]: A tale of two inactivation mechanisms. Neuron. 1995;15:951–960. - PubMed

[6] Baukrowitz T, Yellen G. Modulation of K+ current by frequency and external [K+]: A tale of two inactivation mechanisms. Neuron. 1995;15:951–960. - PubMed

[7] Baukrowitz T, Yellen G. Two functionally distinct subsites for the binding of internal blockers to the pore of voltage-activated K+ channels. Proceedings of the National Academy of Sciences of the USA. 1996;93:13 357–13 361. - PMC - PubMed

[8] Baukrowitz T, Yellen G. Two functionally distinct subsites for the binding of internal blockers to the pore of voltage-activated K+ channels. Proceedings of the National Academy of Sciences of the USA. 1996;93:13 357–13 361. - PMC - PubMed

[9] Blaustein RO, Cole PA, Williams C, Miller C. Tethered blockers as molecular ‘tape measures’ for a voltage-gated K+ channel. Nature Structural Biology. 2000;7:309–311. - PubMed

[10] Blaustein RO, Cole PA, Williams C, Miller C. Tethered blockers as molecular ‘tape measures’ for a voltage-gated K+ channel. Nature Structural Biology. 2000;7:309–311. - PubMed

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Molecular determinants of the inhibition of human Kv1.5 potassium currents by external protons and Zn(2+)

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Molecular determinants of the inhibition of human Kv1.5 potassium currents by external protons and Zn(2+)

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