Activation-dependent subconductance levels in the drk1 K channel suggest a subunit basis for ion permeation and gating.

Ion permeation and channel opening are two fundamental properties of ion channels, the molecular bases of which are poorly understood. Channels can exist in two permeability states, open and closed. The relative amount of time a channel spends in the open conformation depends on the state of activation. In voltage-gated ion channels, activation involves movement of a charged voltage sensor, which is required for channel opening. Single-channel recordings of drk1 K channels expressed in Xenopus oocytes suggested that intermediate current levels (sublevels) may be associated with transitions between the closed and open states. Because K channels are formed by four identical subunits, each contributing to the lining of the pore, it was hypothesized that these sublevels resulted from heteromeric pore conformations. A formal model based on this hypothesis predicted that sublevels should be more frequently observed in partially activated channels, in which some but not all subunits have undergone voltage-dependent conformational changes required for channel opening. Experiments using the drk1 K channel, as well as drk1 channels with mutations in the pore and in the voltage sensor, showed that the probability of visiting a sublevel correlated with voltage- and time-dependent changes in activation. A subunit basis is proposed for channel opening and permeation in which these processes are coupled.

[1]  Christian Rosenmund,et al.  Channel conductance of a AMPA-type glutamate channel is determined by agonist concentration. , 1996 .

[2]  G. Moss,et al.  Rectifying conductance substates in a large conductance Ca(2+)- activated K+ channel: evidence for a fluctuating barrier mechanism , 1996, The Journal of general physiology.

[3]  F. Bezanilla,et al.  Voltage-dependent gating of ionic channels. , 1994, Annual review of biophysics and biomolecular structure.

[4]  Y. Jan,et al.  Alteration of voltage-dependence of Shaker potassium channel by mutations in the S4 sequence , 1991, Nature.

[5]  C. Stevens,et al.  Glutamate activates multiple single channel conductances in hippocampal neurons , 1987, Nature.

[6]  M. Tanouye,et al.  The size of gating charge in wild-type and mutant Shaker potassium channels. , 1992, Science.

[7]  A. Brown,et al.  K+ pore structure revealed by reporter cysteines at inner and outer surfaces , 1995, Neuron.

[8]  T. Schwarz,et al.  Alteration of ionic selectivity of a K+ channel by mutation of the H5 region , 1991, Nature.

[9]  A. VanDongen,et al.  Newly identified brain potassium channels gated by the guanine nucleotide binding protein Go. , 1988, Science.

[10]  H. Matsuda,et al.  Open‐state substructure of inwardly rectifying potassium channels revealed by magnesium block in guinea‐pig heart cells. , 1988, The Journal of physiology.

[11]  E. Moczydlowski,et al.  Subconductance behavior in a maxi Ca2+-activated K+ channel induced by dendrotoxin-I , 1990, Neuron.

[12]  Francisco Bezanilla,et al.  Gating currents from a nonconducting mutant reveal open-closed conformations in Shaker K+ channels , 1993, Neuron.

[13]  E. Isacoff,et al.  Direct Physical Measure of Conformational Rearrangement Underlying Potassium Channel Gating , 1996, Science.

[14]  E. Liman,et al.  Voltage-sensing residues in the S4 region of a mammalian K+ channel , 1991, Nature.

[15]  A. Brown,et al.  Exchange of conduction pathways between two related K+ channels , 1991, Science.

[16]  R. Aldrich,et al.  Shaker potassium channel gating. I: Transitions near the open state , 1994, The Journal of general physiology.

[17]  A. Brown,et al.  Differences between the deep pores of K+ channels determined by an interacting pair of nonpolar amino acids , 1992, Neuron.

[18]  C. Miller,et al.  Silver as a probe of pore-forming residues in a potassium channel. , 1995, Science.

[19]  R. MacKinnon,et al.  Two identical noninteracting sites in an ion channel revealed by proton transfer. , 1994, Science.

[20]  B. Sakmann,et al.  Activation of multiple-conductance state chloride channels in spinal neurones by glycine and GABA , 1983, Nature.

[21]  F. Alvarez-Leefmans,et al.  Chloride Channels and Carriers in Nerve, Muscle, and Glial Cells , 2013, Springer US.

[22]  Gerhard Giebisch,et al.  Multi-barrelled K channels in renal tubules , 1987, Nature.

[23]  N. Unwin Nicotinic acetylcholine receptor at 9 A resolution. , 1993, Journal of molecular biology.

[24]  Singiresu S. Rao,et al.  Optimization Theory and Applications , 1980, IEEE Transactions on Systems, Man, and Cybernetics.

[25]  D. Pietrobon,et al.  Mechanisms of Interaction of Permeant Ions and Protons with Dihydropyridine‐Sensitive Calcium Channels a , 1989, Annals of the New York Academy of Sciences.

[26]  Ehud Y. Isacoff,et al.  Transmembrane Movement of the Shaker K+ Channel S4 , 1996, Neuron.

[27]  R. Aldrich,et al.  Voltage-dependent gating of Shaker A-type potassium channels in Drosophila muscle , 1990, The Journal of general physiology.

[28]  L. Schild,et al.  Permeation of Na+ through open and Zn(2+)-occupied conductance states of cardiac sodium channels modified by batrachotoxin: exploring ion-ion interactions in a multi-ion channel. , 1994, Biophysical journal.

[29]  S. Cull-Candy,et al.  Multiple-conductance channels activated by excitatory amino acids in cerebellar neurons , 1987, Nature.

[30]  Peter Hess,et al.  Conformational changes associated with ion permeation in L-type calcium channels , 1988, Nature.

[31]  Francisco Bezanilla,et al.  Voltage-Sensing Residues in the S2 and S4 Segments of the Shaker K+ Channel , 1996, Neuron.

[32]  J. A. Dani,et al.  Examination of subconductance levels arising from a single ion channel. , 1991, Journal of theoretical biology.

[33]  F. Bezanilla,et al.  S4 mutations alter gating currents of Shaker K channels. , 1994, Biophysical journal.

[34]  T Hoshi,et al.  Shaker potassium channel gating. III: Evaluation of kinetic models for activation , 1994, The Journal of general physiology.

[35]  Yu Huang,et al.  Electrostatic interactions of S4 voltage sensor in shaker K+ channel , 1995, Neuron.

[36]  A. Blatz Chloride Channels in Skeletal Muscle , 1990 .

[37]  C. F. Stevens,et al.  A reinterpretation of mammalian sodium channel gating based on single channel recording , 1983, Nature.

[38]  A. Auerbach,et al.  Flickering of a nicotinic ion channel to a subconductance state. , 1983, Biophysical journal.

[39]  S. Tyerman,et al.  Multiple conductances in the large K+ channel from Chara corallina shown by a transient analysis method. , 1992, Biophysical journal.

[40]  R. MacKinnon,et al.  Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel , 1991, Science.

[41]  M Karplus,et al.  Molecular dynamics simulations of the gramicidin channel. , 1994, Annual review of biophysics and biomolecular structure.

[42]  Peter Hess,et al.  Direct measurement of proton transfer rates to a group controlling the dihydropyridine-sensitive Ca2+ channel , 1987, Nature.

[43]  A. VanDongen,et al.  A new algorithm for idealizing single ion channel data containing multiple unknown conductance levels. , 1996, Biophysical journal.

[44]  A. VanDongen,et al.  A novel potassium channel with delayed rectifier properties isolated from rat brain by expression cloning , 1989, Nature.

[45]  A. VanDongen,et al.  Structural conservation of ion conduction pathways in K channels and glutamate receptors. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[46]  A. Maelicke Nicotinic Acetylcholine Receptor , 1986, NATO ASI Series.

[47]  Y. Jan,et al.  Images of purified Shaker potassium channels , 1994, Current Biology.

[48]  R. Horn,et al.  Molecular Basis of Charge Movement in Voltage-Gated Sodium Channels , 1996, Neuron.

[49]  A. VanDongen,et al.  Alteration and restoration of K+ channel function by deletions at the N- and C-termini , 1990, Neuron.

[50]  R. Aldrich,et al.  Gating of single Shaker potassium channels in Drosophila muscle and in Xenopus oocytes injected with Shaker mRNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[51]  Hirotugu Akaike,et al.  MODERN DEVELOPMENT OF STATISTICAL METHODS , 1981 .

[52]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1952, The Journal of physiology.

[53]  H. Meves,et al.  Multiple conductance states of the sodium channel and of other ion channels. , 1989, Biochimica et biophysica acta.

[54]  D. Baylor,et al.  Conductance and kinetics of single cGMP‐activated channels in salamander rod outer segments. , 1995, The Journal of physiology.

[55]  Pieter Eykhoff,et al.  Trends and progress in system identification , 1981 .

[56]  F J Sigworth,et al.  Voltage gating of ion channels , 1994, Quarterly Reviews of Biophysics.

[57]  K. Magleby,et al.  Opening and closing transitions for BK channels often occur in two steps via sojourns through a brief lifetime subconductance state. , 1993, Biophysical journal.

[58]  B. Nadal-Ginard,et al.  Gating mechanism of a cloned potassium channel expressed in frog oocytes and mammalian cells , 1990, Neuron.

[59]  T Hoshi,et al.  Shaker potassium channel gating. II: Transitions in the activation pathway , 1994, The Journal of general physiology.

[60]  S. Siegelbaum,et al.  Subunit Stoichiometry of Cyclic Nucleotide-Gated Channels and Effects of Subunit Order on Channel Function , 1996, Neuron.

[61]  R. Horn,et al.  Evidence for voltage-dependent S4 movement in sodium channels , 1995, Neuron.