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      Ion Interactions in the High-Affinity Binding Locus of a Voltage-Gated Ca 2+ Channel

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          Abstract

          The selectivity filter of voltage-gated Ca 2+ channels is in part composed of four Glu residues, termed the EEEE locus. Ion selectivity in Ca 2+ channels is based on interactions between permeant ions and the EEEE locus: in a mixture of ions, all of which can pass through the pore when present alone, those ions that bind weakly are impermeant, those that bind more strongly are permeant, and those that bind more strongly yet act as pore blockers as a consequence of their low rate of unbinding from the EEEE locus. Thus, competition among ion species is a determining feature of selectivity filter function in Ca 2+ channels. Previous work has shown that Asp and Ala substitutions in the EEEE locus reduce ion selectivity by weakening ion binding affinity. Here we describe for wild-type and EEEE locus mutants an analysis at the single channel level of competition between Cd 2+, which binds very tightly within the EEEE locus, and Ba 2+ or Li +, which bind less tightly and hence exhibit high flux rates: Cd 2+ binds to the EEEE locus ∼10 4× more tightly than does Ba 2+, and ∼10 8× more tightly than does Li +. For wild-type channels, Cd 2+ entry into the EEEE locus was 400× faster when Li + rather than Ba 2+ was the current carrier, reflecting the large difference between Ba 2+ and Li + in affinity for the EEEE locus. For the substitution mutants, analysis of Cd 2+ block kinetics shows that their weakened ion binding affinity can result from either a reduction in blocker on rate or an enhancement of blocker off rate. Which of these rate effects underlay weakened binding was not specified by the nature of the mutation (Asp vs. Ala), but was instead determined by the valence and affinity of the current-carrying ion (Ba 2+ vs. Li +). The dependence of Cd 2+ block kinetics upon properties of the current-carrying ion can be understood by considering the number of EEEE locus oxygen atoms available to interact with the different ion pairs.

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          Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.

          1. The extracellular patch clamp method, which first allowed the detection of single channel currents in biological membranes, has been further refined to enable higher current resolution, direct membrane patch potential control, and physical isolation of membrane patches. 2. A description of a convenient method for the fabrication of patch recording pipettes is given together with procedures followed to achieve giga-seals i.e. pipette-membrane seals with resistances of 10(9) - 10(11) omega. 3. The basic patch clamp recording circuit, and designs for improved frequency response are described along with the present limitations in recording the currents from single channels. 4. Procedures for preparation and recording from three representative cell types are given. Some properties of single acetylcholine-activated channels in muscle membrane are described to illustrate the improved current and time resolution achieved with giga-seals. 5. A description is given of the various ways that patches of membrane can be physically isolated from cells. This isolation enables the recording of single channel currents with well-defined solutions on both sides of the membrane. Two types of isolated cell-free patch configurations can be formed: an inside-out patch with its cytoplasmic membrane face exposed to the bath solution, and an outside-out patch with its extracellular membrane face exposed to the bath solution. 6. The application of the method for the recording of ionic currents and internal dialysis of small cells is considered. Single channel resolution can be achieved when recording from whole cells, if the cell diameter is small (less than 20 micrometer). 7. The wide range of cell types amenable to giga-seal formation is discussed.
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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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              The potassium permeability of a giant nerve fibre.

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                Author and article information

                Contributors
                Journal
                J Gen Physiol
                The Journal of General Physiology
                The Rockefeller University Press
                0022-1295
                1540-7748
                1 October 2000
                : 116
                : 4
                : 569-586
                Affiliations
                [a ]Department of Pharmacology and Neuroscience Center, University of Colorado Health Sciences Center, Denver, Colorado 80262
                Article
                8228
                10.1085/jgp.116.4.569
                2230626
                11004206
                a2896db6-80fd-4797-9e27-a9ff02f51589
                © 2000 The Rockefeller University Press
                History
                : 8 May 2000
                : 31 August 2000
                : 1 September 2000
                Categories
                Original Article

                Anatomy & Physiology
                permeability,selectivity,site-directed mutagenesis,ion channel
                Anatomy & Physiology
                permeability, selectivity, site-directed mutagenesis, ion channel

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