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10.1016/S0006-3495(96)79268-8

http://scihub22266oqcxt.onion/10.1016/S0006-3495(96)79268-8
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8842207!1233525!8842207
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suck abstract from ncbi


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pmid8842207      Biophys+J 1996 ; 71 (2): 682-94
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  • K+ dependence of open-channel conductance in cloned inward rectifier potassium channels (IRK1, Kir2 1) #MMPMID8842207
  • Lopatin AN; Nichols CG
  • Biophys J 1996[Aug]; 71 (2): 682-94 PMID8842207show ga
  • Potassium conduction through unblocked inwardly rectifying (IRK1, Kir2.1) potassium channels was measured in inside-out-patches from Xenopus oocytes, after removal of polyamine-induced strong inward rectification. Unblocked IRK1 channel current-voltage (I-V) relations show very mild inward rectification in symmetrical solutions, are linearized in nonsymmetrical solutions that bring the K+ reversal potential to extreme negative values, and follow Goldman-Hodgkin-Katz constant field equation at extreme positive E alpha. When intracellular K+ concentration (KIN) was varied, at constant extracellular K+ concentration (KOUT) the conductance at the reversal potential (GREV) followed closely the predictions of the Goldman-Hodgkin-Katz constant field equation at low concentrations and saturated sharply at concentrations of > 150 mM. Similarly, when KOUT was varied, at constant KIN, GREV saturated at concentrations of > 150 mM. A square-root dependence of conductance on KOUT is a well-known property of inward rectifier potassium channels and is a property of the open channel. A nonsymmetrical two-site three-barrier model can qualitatively explain both the I-V relations and the [K+] dependence of conductance of open IRK1 (Kir2.1) channels.
  • |*Potassium Channels, Inwardly Rectifying[MESH]
  • |Animals[MESH]
  • |Cloning, Molecular[MESH]
  • |Female[MESH]
  • |In Vitro Techniques[MESH]
  • |Ion Channel Gating[MESH]
  • |Kinetics[MESH]
  • |Magnesium/pharmacology[MESH]
  • |Mathematics[MESH]
  • |Membrane Potentials/drug effects[MESH]
  • |Models, Biological[MESH]
  • |Oocytes/physiology[MESH]
  • |Patch-Clamp Techniques[MESH]
  • |Polyamines/pharmacology[MESH]
  • |Potassium Channels/biosynthesis/drug effects/*physiology[MESH]
  • |Potassium/*metabolism/pharmacology[MESH]
  • |Recombinant Proteins/biosynthesis/drug effects/metabolism[MESH]


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