Abstract
1. The delayed rectifier (DR) K+ channel pore was probed using different permeant and blocking ions applied intra- and extracellularly. Currents were recorded from bullfrog sympathetic neurons using whole-cell patch-clamp techniques. 2. With intra- and extracellular Cs+ (0 K+), there were large, tetraethylammonium (TEA)-sensitive currents. Adding K+ back to the extracellular solution revealed that the current with Cs+i was K+ selective (permeability ratio PCs/PK = 0.17 +/- 0.02, n = 4) and showed a strong anomalous mole fraction effect. 3. There were also large non-inactivating currents with Na+i and Na+o (0 K+). The current with Na+i was K+ selective (Na+o vs. K+o: PNa/PK = 0.022 +/- 0.005, n = 5), and was TEA sensitive with K+o but not with Na+o. 4. Permeant ions affected gating kinetics. DR currents activated faster in K+ than in Cs+, and activated faster with increasing concentrations of either K+ or Cs+. Deactivation was slowed by increased K+ or Cs+ concentration, with no difference between K+ and Cs+. 5. The pore was also characterized using intracellular blocking ions. A wide variety of monovalent cations (TEA, N-methyl-D-glucamine, arginine, choline, CH3NH3+, Li+, Cs+ and Na+) blocked DR channels from the inside in a voltage-dependent manner: KD at 0 mV was 2.9 mM for TEA and 134-487 mM for the others, at apparent electrical distances (delta) of 0.33-0.79. There was no detectable block by 10 mM Mgi2+. Apart from TEA, the organic cations did not block from the outside. 6. The permeability to Na+ in the absence of K+, and the strong anomalous mole fraction effects observed for Cs+o + K+o mixtures, suggest that DR channels select for K+ using ion-ion competition. The block by large intracellular cations shows that the pore is asymmetrical. The loss of high affinity TEAo block with Na+i and Na+o, and the effects of permeant ions on gating, suggest that channel conformation may be affected by ions in the pore.
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Selected References
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- Adams P. R., Brown D. A., Constanti A. M-currents and other potassium currents in bullfrog sympathetic neurones. J Physiol. 1982 Sep;330:537–572. doi: 10.1113/jphysiol.1982.sp014357. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Armstrong C. M. Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons. J Gen Physiol. 1971 Oct;58(4):413–437. doi: 10.1085/jgp.58.4.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Armstrong C. M., Neyton J. Ion permeation through calcium channels. A one-site model. Ann N Y Acad Sci. 1991;635:18–25. doi: 10.1111/j.1749-6632.1991.tb36477.x. [DOI] [PubMed] [Google Scholar]
- Barry P. H., Lynch J. W. Liquid junction potentials and small cell effects in patch-clamp analysis. J Membr Biol. 1991 Apr;121(2):101–117. doi: 10.1007/BF01870526. [DOI] [PubMed] [Google Scholar]
- Bezanilla F., Armstrong C. M. Negative conductance caused by entry of sodium and cesium ions into the potassium channels of squid axons. J Gen Physiol. 1972 Nov;60(5):588–608. doi: 10.1085/jgp.60.5.588. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Block B. M., Jones S. W. Ion permeation and block of M-type and delayed rectifier potassium channels. Whole-cell recordings from bullfrog sympathetic neurons. J Gen Physiol. 1996 Apr;107(4):473–488. doi: 10.1085/jgp.107.4.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Callahan M. J., Korn S. J. Permeation of Na+ through a delayed rectifier K+ channel in chick dorsal root ganglion neurons. J Gen Physiol. 1994 Oct;104(4):747–771. doi: 10.1085/jgp.104.4.747. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cecchi X., Wolff D., Alvarez O., Latorre R. Mechanisms of Cs+ blockade in a Ca2+-activated K+ channel from smooth muscle. Biophys J. 1987 Nov;52(5):707–716. doi: 10.1016/S0006-3495(87)83265-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Choi K. L., Mossman C., Aubé J., Yellen G. The internal quaternary ammonium receptor site of Shaker potassium channels. Neuron. 1993 Mar;10(3):533–541. doi: 10.1016/0896-6273(93)90340-w. [DOI] [PubMed] [Google Scholar]
- Cukierman S., Yellen G., Miller C. The K+ channel of sarcoplasmic reticulum. A new look at Cs+ block. Biophys J. 1985 Sep;48(3):477–484. doi: 10.1016/S0006-3495(85)83803-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Demo S. D., Yellen G. Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore. Biophys J. 1992 Mar;61(3):639–648. doi: 10.1016/S0006-3495(92)81869-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fabiato A., Fabiato F. Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells. J Physiol (Paris) 1979;75(5):463–505. [PubMed] [Google Scholar]
- French R. J., Shoukimas J. J. An ion's view of the potassium channel. The structure of the permeation pathway as sensed by a variety of blocking ions. J Gen Physiol. 1985 May;85(5):669–698. doi: 10.1085/jgp.85.5.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- French R. J., Shoukimas J. J. Blockage of squid axon potassium conductance by internal tetra-N-alkylammonium ions of various sizes. Biophys J. 1981 May;34(2):271–291. doi: 10.1016/S0006-3495(81)84849-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- French R. J., Wells J. B. Sodium ions as blocking agents and charge carriers in the potassium channel of the squid giant axon. J Gen Physiol. 1977 Dec;70(6):707–724. doi: 10.1085/jgp.70.6.707. [DOI] [PMC free article] [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]
- Ikeda S. R., Korn S. J. Influence of permeating ions on potassium channel block by external tetraethylammonium. J Physiol. 1995 Jul 15;486(Pt 2):267–272. doi: 10.1113/jphysiol.1995.sp020809. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones S. W. Sodium currents in dissociated bull-frog sympathetic neurones. J Physiol. 1987 Aug;389:605–627. doi: 10.1113/jphysiol.1987.sp016674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones S. W. Time course of receptor-channel coupling in frog sympathetic neurons. Biophys J. 1991 Aug;60(2):502–507. doi: 10.1016/S0006-3495(91)82077-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Korn S. J., Ikeda S. R. Permeation selectivity by competition in a delayed rectifier potassium channel. Science. 1995 Jul 21;269(5222):410–412. doi: 10.1126/science.7618108. [DOI] [PubMed] [Google Scholar]
- Kuffler S. W., Sejnowski T. J. Peptidergic and muscarinic excitation at amphibian sympathetic synapses. J Physiol. 1983 Aug;341:257–278. doi: 10.1113/jphysiol.1983.sp014805. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lopatin A. N., Nichols C. G. Internal Na+ and Mg2+ blockade of DRK1 (Kv2.1) potassium channels expressed in Xenopus oocytes. Inward rectification of a delayed rectifier. J Gen Physiol. 1994 Feb;103(2):203–216. doi: 10.1085/jgp.103.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matteson D. R., Swenson R. P., Jr External monovalent cations that impede the closing of K channels. J Gen Physiol. 1986 May;87(5):795–816. doi: 10.1085/jgp.87.5.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neher E. Correction for liquid junction potentials in patch clamp experiments. Methods Enzymol. 1992;207:123–131. doi: 10.1016/0076-6879(92)07008-c. [DOI] [PubMed] [Google Scholar]
- Neyton J., Pelleschi M. Multi-ion occupancy alters gating in high-conductance, Ca(2+)-activated K+ channels. J Gen Physiol. 1991 Apr;97(4):641–665. doi: 10.1085/jgp.97.4.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shapiro M. S., DeCoursey T. E. Permeant ion effects on the gating kinetics of the type L potassium channel in mouse lymphocytes. J Gen Physiol. 1991 Jun;97(6):1251–1278. doi: 10.1085/jgp.97.6.1251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stampe P., Begenisich T. Unidirectional K+ fluxes through recombinant Shaker potassium channels expressed in single Xenopus oocytes. J Gen Physiol. 1996 Apr;107(4):449–457. doi: 10.1085/jgp.107.4.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Swenson R. P., Jr, Armstrong C. M. K+ channels close more slowly in the presence of external K+ and Rb+. Nature. 1981 Jun 4;291(5814):427–429. doi: 10.1038/291427a0. [DOI] [PubMed] [Google Scholar]
- Taglialatela M., Vandongen A. M., Drewe J. A., Joho R. H., Brown A. M., Kirsch G. E. Patterns of internal and external tetraethylammonium block in four homologous K+ channels. Mol Pharmacol. 1991 Aug;40(2):299–307. [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]
- Yang J., Ellinor P. T., Sather W. A., Zhang J. F., Tsien R. W. Molecular determinants of Ca2+ selectivity and ion permeation in L-type Ca2+ channels. Nature. 1993 Nov 11;366(6451):158–161. doi: 10.1038/366158a0. [DOI] [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]
- Zhu Y., Ikeda S. R. Anomalous permeation of Na+ through a putative K+ channel in rat superior cervical ganglion neurones. J Physiol. 1993 Aug;468:441–461. doi: 10.1113/jphysiol.1993.sp019781. [DOI] [PMC free article] [PubMed] [Google Scholar]