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      Mechanism of the Voltage Sensitivity of IRK1 Inward-rectifier K + Channel Block by the Polyamine Spermine

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          Abstract

          IRK1 (Kir2.1) inward-rectifier K + channels exhibit exceedingly steep rectification, which reflects strong voltage dependence of channel block by intracellular cations such as the polyamine spermine. On the basis of studies of IRK1 block by various amine blockers, it was proposed that the observed voltage dependence (valence ∼5) of IRK1 block by spermine results primarily from K + ions, not spermine itself, traversing the transmembrane electrical field that drops mostly across the narrow ion selectivity filter, as spermine and K + ions displace one another during channel block and unblock. If indeed spermine itself only rarely penetrates deep into the ion selectivity filter, then a long blocker with head groups much wider than the selectivity filter should exhibit comparably strong voltage dependence. We confirm here that channel block by two molecules of comparable length, decane- bis-trimethylammonium (bis-QA C10) and spermine, exhibit practically identical overall voltage dependence even though the head groups of the former are much wider (∼6 Å) than the ion selectivity filter (∼3 Å). For both blockers, the overall equilibrium dissociation constant differs from the ratio of apparent rate constants of channel unblock and block. Also, although steady-state IRK1 block by both cations is strongly voltage dependent, their apparent channel-blocking rate constant exhibits minimal voltage dependence, which suggests that the pore becomes blocked as soon as the blocker encounters the innermost K + ion. These findings strongly suggest the existence of at least two (potentially identifiable) sequentially related blocked states with increasing numbers of K + ions displaced. Consequently, the steady-state voltage dependence of IRK1 block by spermine or bis-QA C10 should increase with membrane depolarization, a prediction indeed observed. Further kinetic analysis identifies two blocked states, and shows that most of the observed steady-state voltage dependence is associated with the transition between blocked states, consistent with the view that the mutual displacement of blocker and K + ions must occur mainly as the blocker travels along the long inner pore.

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          Most cited references38

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          Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.

          The subunit stoichiometry of the mammalian K+ channel KV1.1 (RCK1) was examined by linking together the coding sequences of 2-5 K+ channel subunits in a single open reading frame and tagging the expression of individual subunits with a mutation (Y379K or Y379R) that altered the sensitivity of the channel to block by external tetraethylammonium ion. Two lines of evidence argue that these constructs lead to K+ channel expression only through the formation of functional tetramers. First, currents expressed by tetrameric constructs containing a single mutant subunit have a sensitivity to tetraethylammonium that is well fitted by a single site binding isotherm. Second, a mutant subunit (Y379K) that expresses only as part of a heteromultimer contributes to the expression of functional channels when coexpressed with a trimeric construct but not a tetrameric construct.
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            Crystal structure of the potassium channel KirBac1.1 in the closed state.

            The KirBac1.1 channel belongs to the inward-rectifier family of potassium channels. Here we report the structure of the entire prokaryotic Kir channel assembly, in the closed state, refined to a resolution of 3.65 angstroms. We identify the main activation gate and structural elements involved in gating. On the basis of structural evidence presented here, we suggest that gating involves coupling between the intracellular and membrane domains. This further suggests that initiation of gating by membrane or intracellular signals represents different entry points to a common mechanistic pathway.
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              Primary structure and functional expression of a mouse inward rectifier potassium channel.

              A complementary DNA encoding an inward rectifier K+ channel (IRK1) was isolated from a mouse macrophage cell line by expression cloning. This channel conducts inward K+ current below the K+ equilibrium potential but passes little outward K+ current. The IRK1 channel contains only two putative transmembrane segments per subunit and corresponds to the inner core structure of voltage-gated K+ channels. The IRK1 channel and an ATP-regulated K+ channel show extensive sequence similarity and constitute a new superfamily.
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                Author and article information

                Journal
                J Gen Physiol
                The Journal of General Physiology
                The Rockefeller University Press
                0022-1295
                1540-7748
                April 2005
                : 125
                : 4
                : 413-426
                Affiliations
                Department of Physiology, University of Pennsylvania, Philadelphia, PA 19104
                Author notes

                Correspondence to Zhe Lu: zhelu@ 123456mail.med.upenn.edu

                Article
                200409242
                10.1085/jgp.200409242
                2217510
                15795311
                5c88b655-0d59-4476-92b9-6e6280cb4f0a
                Copyright © 2005, The Rockefeller University Press
                History
                : 20 December 2004
                : 23 February 2005
                Categories
                Article

                Anatomy & Physiology
                quaternary ammonium,valence,kinetics,energetics,kir
                Anatomy & Physiology
                quaternary ammonium, valence, kinetics, energetics, kir

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