Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1975 Jul 1;66(1):47–65. doi: 10.1085/jgp.66.1.47

Magnitude and location of surface charges on Myxicola giant axons

PMCID: PMC2226185  PMID: 1159402

Abstract

The effects of changes in the concentration of calcium in solutions bathing Myxicola giant axons on the voltage dependence of sodium and potassium conductance and on the instantaneous sodium and potassium current-voltage relations have been measured. The sodium conductance- voltage relation is shifted along the voltage axis by 13 mV in the hyperpolarizing direction for a fourfold decrease in calcium concentration. The potassium conductance-voltage relation is shifted only half as much as that for sodium. There is no effect on the shape of the sodium and potassium instantaneous current-voltage curves: the normal constant-field rectification of potassium currents is maintained and the normal linear relationship of sodium currents is maintained. Considering that shifts in conductances would reflect the presence of surface charges near the gating machinery and that shape changes of instantaneous current-voltage curves would reflect the presence of surface charges near the ionic pores, these results indicate a negative surface charge density of about 1 electronic charge per 120 A2 near the sodium gating machinery, about 1 e/300 A2 for the potassium gating machinery, and much less surface charge near the sodium or potassium pores. There may be some specific binding of calcium to these surface charges with an upper limit on the binding constant of about 0.2 M-1. The differences in surface charge density suggest a spatial separation for these four membrane components.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adelman W. J., Jr, Palti Y. The effects of external potassium and long duration voltage conditioning on the amplitude of sodium currents in the giant axon of the squid, Loligo pealei. J Gen Physiol. 1969 Nov;54(5):589–606. doi: 10.1085/jgp.54.5.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Begenisich T., Lynch C. Effects of internal divalent cations on voltage-clamped squid axons. J Gen Physiol. 1974 Jun;63(6):675–689. doi: 10.1085/jgp.63.6.675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Binstock L., Goldman L. Current- and voltage-clamped studies on Myxicola giant axons. Effect of tetrodotoxin. J Gen Physiol. 1969 Dec;54(6):730–740. doi: 10.1085/jgp.54.6.730. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Binstock L., Goldman L. Rectification in instantaneous potassium current-voltage relations in Myxicola giant axons. J Physiol. 1971 Sep;217(3):517–531. doi: 10.1113/jphysiol.1971.sp009583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brismar T. Effects of ionic concentration on permeability properties of nodal membrane in myelinated nerve fibres of Xenopus laevis. Potential clamp experiments. Acta Physiol Scand. 1973 Apr;87(4):474–484. doi: 10.1111/j.1748-1716.1973.tb05414.x. [DOI] [PubMed] [Google Scholar]
  6. COLE K. S., MOORE J. W. Liquid junction and membrane potentials of the squid giant axon. J Gen Physiol. 1960 May;43:971–980. doi: 10.1085/jgp.43.5.971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chandler W. K., Hodgkin A. L., Meves H. The effect of changing the internal solution on sodium inactivation and related phenomena in giant axons. J Physiol. 1965 Oct;180(4):821–836. doi: 10.1113/jphysiol.1965.sp007733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chandler W. K., Meves H. Voltage clamp experiments on internally perfused giant axons. J Physiol. 1965 Oct;180(4):788–820. doi: 10.1113/jphysiol.1965.sp007732. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FRANKENHAEUSER B., HODGKIN A. L. The action of calcium on the electrical properties of squid axons. J Physiol. 1957 Jul 11;137(2):218–244. doi: 10.1113/jphysiol.1957.sp005808. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fishman S. N., Chodorov B. I., Volkenstein M. V. Molecular mechanisms of membrane ionic permeability changes. Biochim Biophys Acta. 1971 Jan 5;225(1):1–10. doi: 10.1016/0005-2736(71)90277-x. [DOI] [PubMed] [Google Scholar]
  11. Goldman L., Schauf C. L. Inactivation of the sodium current in Myxicola giant axons. Evidence for coupling to the activation process. J Gen Physiol. 1972 Jun;59(6):659–675. doi: 10.1085/jgp.59.6.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. HODGKIN A. L., HUXLEY A. F., KATZ B. Measurement of current-voltage relations in the membrane of the giant axon of Loligo. J Physiol. 1952 Apr;116(4):424–448. doi: 10.1113/jphysiol.1952.sp004716. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Henderson R., Ritchie J. M., Strichartz G. R. The binding of labelled saxitoxin to the sodium channels in nerve membranes. J Physiol. 1973 Dec;235(3):783–804. doi: 10.1113/jphysiol.1973.sp010417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hille B. Charges and potentials at the nerve surface. Divalent ions and pH. J Gen Physiol. 1968 Feb;51(2):221–236. doi: 10.1085/jgp.51.2.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hille B. Potassium channels in myelinated nerve. Selective permeability to small cations. J Gen Physiol. 1973 Jun;61(6):669–686. doi: 10.1085/jgp.61.6.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hille B. The permeability of the sodium channel to organic cations in myelinated nerve. J Gen Physiol. 1971 Dec;58(6):599–619. doi: 10.1085/jgp.58.6.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. McLaughlin S. G., Szabo G., Eisenman G. Divalent ions and the surface potential of charged phospholipid membranes. J Gen Physiol. 1971 Dec;58(6):667–687. doi: 10.1085/jgp.58.6.667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Moore L. E., Jakobsson E. Interpretation of the sodium permeability changes of myelinated nerve in terms of linear relaxation theory. J Theor Biol. 1971 Oct;33(1):77–89. doi: 10.1016/0022-5193(71)90217-7. [DOI] [PubMed] [Google Scholar]
  19. Rojas E., Atwater I. An experimental approach to determine membrane charges in squid giant axons. J Gen Physiol. 1968 May;51(5 Suppl):131S+–131S+. [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES