Abstract
L-type Ca channels from porcine cardiac sarcolemma were incorporated into planar lipid bilayers. We characterized interactions of permeant and blocking ions with the channel's pore by (a) studying the current- voltage relationships for Ca2+ and Na+ when equal concentrations of the ions were present in both internal and external solutions, (b) testing the dose-dependent block of Ba2+ currents through the channels by internally applied cadmium, and (c) examining the dose and voltage dependence of the block of Na+ currents through the channels by internally and externally applied Ca2+. We found that the I-V relationship for Na+ appears symmetrical through the origin when equal concentrations of Na+ are present on both sides of the channel (gamma = 90 pS in 200 mM NaCl). The conductance for outward Ca2+ currents with 100 mM Ca2+ on both sides of the channel is approximately 8 pS, a value identical to that observed for inward currents when 100 mM Ca2+ was present outside only. This provides evidence that ions pass through the channel equally well regardless of the direction of net flux. In addition, we find that internal Cd2+ is as effective as external Cd2+ in blocking Ba2+ currents through the channels, again suggesting identical interactions of ions with each end of the pore. Finally, we find that micromolar Ca2+, either in the internal or in the external solution, blocks Na+ currents through the channels. The affinity for internally applied Ca2+ appears the same as that for externally applied Ca2+. The voltage dependence of the Ca(2+)-block suggests that the sites to which Ca2+ binds are located approximately 15% and approximately 85% of the electric field into the pore. Taken together, these data provide direct experimental evidence for the existence of at least two ion binding sites with high affinity for Ca2+, and support the idea that the sites are symmetrically located within the electric field across L-type Ca channels.
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- Almers W., McCleskey E. W. Non-selective conductance in calcium channels of frog muscle: calcium selectivity in a single-file pore. J Physiol. 1984 Aug;353:585–608. doi: 10.1113/jphysiol.1984.sp015352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almers W., McCleskey E. W., Palade P. T. A non-selective cation conductance in frog muscle membrane blocked by micromolar external calcium ions. J Physiol. 1984 Aug;353:565–583. doi: 10.1113/jphysiol.1984.sp015351. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Byerly L., Chase P. B., Stimers J. R. Permeation and interaction of divalent cations in calcium channels of snail neurons. J Gen Physiol. 1985 Apr;85(4):491–518. doi: 10.1085/jgp.85.4.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Campbell D. L., Giles W. R., Hume J. R., Noble D., Shibata E. F. Reversal potential of the calcium current in bull-frog atrial myocytes. J Physiol. 1988 Sep;403:267–286. doi: 10.1113/jphysiol.1988.sp017249. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Campbell D. L., Giles W. R., Hume J. R., Shibata E. F. Inactivation of calcium current in bull-frog atrial myocytes. J Physiol. 1988 Sep;403:287–315. doi: 10.1113/jphysiol.1988.sp017250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Campbell D. L., Rasmusson R. L., Strauss H. C. Theoretical study of the voltage and concentration dependence of the anomalous mole fraction effect in single calcium channels. New insights into the characterization of multi-ion channels. Biophys J. 1988 Nov;54(5):945–954. doi: 10.1016/S0006-3495(88)83030-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coronado R., Affolter H. Insulation of the conduction pathway of muscle transverse tubule calcium channels from the surface charge of bilayer phospholipid. J Gen Physiol. 1986 Jun;87(6):933–953. doi: 10.1085/jgp.87.6.933. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dani J. A. Ion-channel entrances influence permeation. Net charge, size, shape, and binding considerations. Biophys J. 1986 Mar;49(3):607–618. doi: 10.1016/S0006-3495(86)83688-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehrlich B. E., Schen C. R., Garcia M. L., Kaczorowski G. J. Incorporation of calcium channels from cardiac sarcolemmal membrane vesicles into planar lipid bilayers. Proc Natl Acad Sci U S A. 1986 Jan;83(1):193–197. doi: 10.1073/pnas.83.1.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Friel D. D., Tsien R. W. Voltage-gated calcium channels: direct observation of the anomalous mole fraction effect at the single-channel level. Proc Natl Acad Sci U S A. 1989 Jul;86(13):5207–5211. doi: 10.1073/pnas.86.13.5207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fukushima Y., Hagiwara S. Currents carried by monovalent cations through calcium channels in mouse neoplastic B lymphocytes. J Physiol. 1985 Jan;358:255–284. doi: 10.1113/jphysiol.1985.sp015550. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hadley R. W., Hume J. R. An intrinsic potential-dependent inactivation mechanism associated with calcium channels in guinea-pig myocytes. J Physiol. 1987 Aug;389:205–222. doi: 10.1113/jphysiol.1987.sp016654. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hess P., Lansman J. B., Tsien R. W. Calcium channel selectivity for divalent and monovalent cations. Voltage and concentration dependence of single channel current in ventricular heart cells. J Gen Physiol. 1986 Sep;88(3):293–319. doi: 10.1085/jgp.88.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hess P., Prod'Hom B., Pietrobon D. Mechanisms of interaction of permeant ions and protons with dihydropyridine-sensitive calcium channels. Ann N Y Acad Sci. 1989;560:80–93. doi: 10.1111/j.1749-6632.1989.tb24082.x. [DOI] [PubMed] [Google Scholar]
- Hess P., Tsien R. W. Mechanism of ion permeation through calcium channels. 1984 May 31-Jun 6Nature. 309(5967):453–456. doi: 10.1038/309453a0. [DOI] [PubMed] [Google Scholar]
- Huang Y., Quayle J. M., Worley J. F., Standen N. B., Nelson M. T. External cadmium and internal calcium block of single calcium channels in smooth muscle cells from rabbit mesenteric artery. Biophys J. 1989 Nov;56(5):1023–1028. doi: 10.1016/S0006-3495(89)82747-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kostyuk P. G., Mironov S. L. Some predictions concerning the calcium channel model with different conformational states. Gen Physiol Biophys. 1986 Dec;5(6):649–654. [PubMed] [Google Scholar]
- Kretsinger R. H., Barry C. D. The predicted structure of the calcium-binding component of troponin. Biochim Biophys Acta. 1975 Sep 9;405(1):40–52. doi: 10.1016/0005-2795(75)90312-8. [DOI] [PubMed] [Google Scholar]
- Lansman J. B. Blockade of current through single calcium channels by trivalent lanthanide cations. Effect of ionic radius on the rates of ion entry and exit. J Gen Physiol. 1990 Apr;95(4):679–696. doi: 10.1085/jgp.95.4.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lansman J. B., Hess P., Tsien R. W. Blockade of current through single calcium channels by Cd2+, Mg2+, and Ca2+. Voltage and concentration dependence of calcium entry into the pore. J Gen Physiol. 1986 Sep;88(3):321–347. doi: 10.1085/jgp.88.3.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee K. S., Tsien R. W. High selectivity of calcium channels in single dialysed heart cells of the guinea-pig. J Physiol. 1984 Sep;354:253–272. doi: 10.1113/jphysiol.1984.sp015374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McDonald T. F., Cavalié A., Trautwein W., Pelzer D. Voltage-dependent properties of macroscopic and elementary calcium channel currents in guinea pig ventricular myocytes. Pflugers Arch. 1986 May;406(5):437–448. doi: 10.1007/BF00583365. [DOI] [PubMed] [Google Scholar]
- Pietrobon D., Prod'hom B., Hess P. Conformational changes associated with ion permeation in L-type calcium channels. Nature. 1988 May 26;333(6171):373–376. doi: 10.1038/333373a0. [DOI] [PubMed] [Google Scholar]
- Pietrobon D., Prod'hom B., Hess P. Interactions of protons with single open L-type calcium channels. pH dependence of proton-induced current fluctuations with Cs+, K+, and Na+ as permeant ions. J Gen Physiol. 1989 Jul;94(1):1–21. doi: 10.1085/jgp.94.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosenberg R. L., Hess P., Reeves J. P., Smilowitz H., Tsien R. W. Calcium channels in planar lipid bilayers: insights into mechanisms of ion permeation and gating. Science. 1986 Mar 28;231(4745):1564–1566. doi: 10.1126/science.2420007. [DOI] [PubMed] [Google Scholar]
- Rosenberg R. L., Hess P., Tsien R. W. Cardiac calcium channels in planar lipid bilayers. L-type channels and calcium-permeable channels open at negative membrane potentials. J Gen Physiol. 1988 Jul;92(1):27–54. doi: 10.1085/jgp.92.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Toyoshima C., Unwin N. Ion channel of acetylcholine receptor reconstructed from images of postsynaptic membranes. Nature. 1988 Nov 17;336(6196):247–250. doi: 10.1038/336247a0. [DOI] [PubMed] [Google Scholar]
- Tsien R. W., Hess P., McCleskey E. W., Rosenberg R. L. Calcium channels: mechanisms of selectivity, permeation, and block. Annu Rev Biophys Biophys Chem. 1987;16:265–290. doi: 10.1146/annurev.bb.16.060187.001405. [DOI] [PubMed] [Google Scholar]
- Woodhull A. M. Ionic blockage of sodium channels in nerve. J Gen Physiol. 1973 Jun;61(6):687–708. doi: 10.1085/jgp.61.6.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yellen G. Ionic permeation and blockade in Ca2+-activated K+ channels of bovine chromaffin cells. J Gen Physiol. 1984 Aug;84(2):157–186. doi: 10.1085/jgp.84.2.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yue D. T., Marban E. Permeation in the dihydropyridine-sensitive calcium channel. Multi-ion occupancy but no anomalous mole-fraction effect between Ba2+ and Ca2+. J Gen Physiol. 1990 May;95(5):911–939. doi: 10.1085/jgp.95.5.911. [DOI] [PMC free article] [PubMed] [Google Scholar]
