Literature DB >> 18708455

Anion-cation permeability correlates with hydrated counterion size in glycine receptor channels.

Silas Sugiharto1, Trevor M Lewis, Andrew J Moorhouse, Peter R Schofield, Peter H Barry.   

Abstract

The functional role of ligand-gated ion channels depends critically on whether they are predominantly permeable to cations or anions. However, these, and other ion channels, are not perfectly selective, allowing some counterions to also permeate. To address the mechanisms by which such counterion permeation occurs, we measured the anion-cation permeabilities of different alkali cations, Li(+) Na(+), and Cs(+), relative to either Cl(-) or NO(3)(-) anions in both a wild-type glycine receptor channel (GlyR) and a mutant GlyR with a wider pore diameter. We hypothesized and showed that counterion permeation in anionic channels correlated inversely with an equivalent or effective hydrated size of the cation relative to the channel pore radius, with larger counterion permeabilities being observed in the wider pore channel. We also showed that the anion component of conductance was independent of the nature of the cation. We suggest that anions and counterion cations can permeate through the pore as neutral ion pairs, to allow the cations to overcome the large energy barriers resulting from the positively charged selectivity filter in small GlyR channels, with the permeability of such ion pairs being dependent on the effective hydrated diameter of the ion pair relative to the pore diameter.

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Year:  2008        PMID: 18708455      PMCID: PMC2576370          DOI: 10.1529/biophysj.107.125690

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  28 in total

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2.  Cation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.

Authors:  Angelo Keramidas; Andrew J Moorhouse; Kerrie D Pierce; Peter R Schofield; Peter H Barry
Journal:  J Gen Physiol       Date:  2002-05       Impact factor: 4.086

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Authors:  Jane E Carland; Andrew J Moorhouse; Peter H Barry; Graham A R Johnston; Mary Chebib
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Review 4.  Liquid junction potentials and small cell effects in patch-clamp analysis.

Authors:  P H Barry; J W Lynch
Journal:  J Membr Biol       Date:  1991-04       Impact factor: 1.843

5.  A theory of ion permeation through membranes with fixed neutral sites.

Authors:  P H Barry; J M Diamond
Journal:  J Membr Biol       Date:  1971-12       Impact factor: 1.843

6.  The strychnine-binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptors.

Authors:  G Grenningloh; A Rienitz; B Schmitt; C Methfessel; M Zensen; K Beyreuther; E D Gundelfinger; H Betz
Journal:  Nature       Date:  1987 Jul 16-22       Impact factor: 49.962

7.  JPCalc, a software package for calculating liquid junction potential corrections in patch-clamp, intracellular, epithelial and bilayer measurements and for correcting junction potential measurements.

Authors:  P H Barry
Journal:  J Neurosci Methods       Date:  1994-01       Impact factor: 2.390

8.  Membrane potentials at zero current. The significance of a constant ionic permeability ratio.

Authors:  J P Sandblom; G Eisenman
Journal:  Biophys J       Date:  1967-05       Impact factor: 4.033

9.  Charge scan reveals an extended region at the intracellular end of the GABA receptor pore that can influence ion selectivity.

Authors:  Virginia E Wotring; David S Weiss
Journal:  J Gen Physiol       Date:  2007-12-17       Impact factor: 4.086

10.  A high-conductance anion channel in adult amphibian skeletal muscle.

Authors:  K H Woll; M D Leibowitz; B Neumcke; B Hille
Journal:  Pflugers Arch       Date:  1987-12       Impact factor: 3.657

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Authors:  Silas Sugiharto; Jane E Carland; Trevor M Lewis; Andrew J Moorhouse; Peter H Barry
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Authors:  Sebastian Jojoa-Cruz; Kei Saotome; Che Chun Alex Tsui; Wen-Hsin Lee; Mark S P Sansom; Swetha E Murthy; Ardem Patapoutian; Andrew B Ward
Journal:  Nat Commun       Date:  2022-02-14       Impact factor: 14.919

5.  Functional characterization of the cardiac ryanodine receptor pore-forming region.

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  5 in total

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