» Articles » PMID: 8037798

Ion Permeation, Divalent Ion Block, and Chemical Modification of Single Sodium Channels. Description by Single- and Double-occupancy Rate-theory Models

Overview
Journal J Gen Physiol
Specialty Physiology
Date 1994 Mar 1
PMID 8037798
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Calcium ions, applied internally, externally, or symmetrically, have been used in conjunction with rate-theory modeling to explore the energy profile of the ion-conducting pore of sodium channels. The block, by extracellular and/or intracellular calcium, of sodium ion conduction through single, batrachotoxin-activated sodium channels from rat brain was studied in planar lipid bilayers. Extracellular calcium caused a reduction of inward current that was enhanced by hyperpolarization and a weaker block of outward current. Intracellular calcium reduced both outward and inward sodium current, with the block being weakly dependent on voltage and enhanced by depolarization. These results, together with the dependence of single-channel conductance on sodium concentration, and the effects of symmetrically applied calcium, were described using single- or double-occupancy, three-barrier, two-site (3B2S), or single-occupancy, 4B3S rate-theory models. There appear to be distinct outer and inner regions of the channel, easily accessed by external or internal calcium respectively, separated by a rate-limiting barrier to calcium permeation. Most of the data could be well fit by each of the models. Reducing the ion interaction energies sufficiently to allow a small but significant probability of two-ion occupancy in the 3B2S model yielded better overall fits than for either 3B2S or 4B3S models constrained to single occupancy. The outer ion-binding site of the model may represent a section of the pore in which sodium, calcium, and guanidinium toxins, such as saxitoxin or tetrodotoxin, compete. Under physiological conditions, with millimolar calcium externally, and high potassium internally, the model channels are occupied by calcium or potassium much of the time, causing a significant reduction in single-channel conductance from the value measured with sodium as the only cation species present. Sodium conductance and degree of block by external calcium are reduced by modification of single channels with the carboxyl reagent, trimethyloxonium (TMO) (Worley et al., 1986) Journal of General Physiology. 87:327-349). Elevations of only the outermost parts of the energy profiles for sodium and calcium were sufficient to account for the reductions in conductance and in efficacy of calcium block produced by TMO modification.

Citing Articles

Molecular Dynamics Simulations of Ion Permeation in Human Voltage-Gated Sodium Channels.

Alberini G, Paz S, Corradi B, Abrams C, Benfenati F, Maragliano L J Chem Theory Comput. 2023; 19(10):2953-2972.

PMID: 37116214 PMC: 10210251. DOI: 10.1021/acs.jctc.2c00990.


Bases of Bacterial Sodium Channel Selectivity Among Organic Cations.

Wang Y, Finol-Urdaneta R, Ngo V, French R, Noskov S Sci Rep. 2019; 9(1):15260.

PMID: 31649292 PMC: 6813354. DOI: 10.1038/s41598-019-51605-y.


Selective ion permeation involves complexation with carboxylates and lysine in a model human sodium channel.

Flood E, Boiteux C, Allen T PLoS Comput Biol. 2018; 14(9):e1006398.

PMID: 30208027 PMC: 6152994. DOI: 10.1371/journal.pcbi.1006398.


Comparison of permeation mechanisms in sodium-selective ion channels.

Boiteux C, Flood E, Allen T Neurosci Lett. 2018; 700:3-8.

PMID: 29807068 PMC: 6592624. DOI: 10.1016/j.neulet.2018.05.036.


The hitchhiker's guide to the voltage-gated sodium channel galaxy.

Ahern C, Payandeh J, Bosmans F, Chanda B J Gen Physiol. 2015; 147(1):1-24.

PMID: 26712848 PMC: 4692491. DOI: 10.1085/jgp.201511492.


References
1.
Butler J . The thermodynamic activity of calcium ion in sodium chloride-calcium chloride electrolytes. Biophys J. 1968; 8(12):1426-33. PMC: 1367446. DOI: 10.1016/S0006-3495(68)86564-6. View

2.
Wu J . Dynamic ion-ion and water-ion interactions in ion channels. Biophys J. 1992; 61(5):1316-31. PMC: 1260395. DOI: 10.1016/S0006-3495(92)81940-9. View

3.
Green W, WEISS L, Andersen O . Batrachotoxin-modified sodium channels in planar lipid bilayers. Characterization of saxitoxin- and tetrodotoxin-induced channel closures. J Gen Physiol. 1987; 89(6):873-903. PMC: 2215969. DOI: 10.1085/jgp.89.6.873. View

4.
Begenisich T, Danko M . Hydrogen ion block of the sodium pore in squid giant axons. J Gen Physiol. 1983; 82(5):599-618. PMC: 2228713. DOI: 10.1085/jgp.82.5.599. View

5.
Mackinnon R, Miller C . Mutant potassium channels with altered binding of charybdotoxin, a pore-blocking peptide inhibitor. Science. 1989; 245(4924):1382-5. DOI: 10.1126/science.2476850. View