Literature DB >> 10653890

The intrinsic electrostatic potential and the intermediate ring of charge in the acetylcholine receptor channel.

G G Wilson1, J M Pascual, N Brooijmans, D Murray, A Karlin.   

Abstract

A ring of aligned glutamate residues named the intermediate ring of charge surrounds the intracellular end of the acetylcholine receptor channel and dominates cation conduction (Imoto et al. 1988). Four of the five subunits in mouse-muscle acetylcholine receptor contribute a glutamate to the ring. These glutamates were mutated to glutamine or lysine, and combinations of mutant and native subunits, yielding net ring charges of -1 to -4, were expressed in Xenopus laevis oocytes. In all complexes, the alpha subunit contained a Cys substituted for alphaThr244, three residues away from the ring glutamate alphaGlu241. The rate constants for the reactions of alphaThr244Cys with the neutral 2-hydroxyethyl-methanethiosulfonate, the positively charged 2-ammonioethyl-methanethiosulfonate, and the doubly positively charged 2-ammonioethyl-2'-ammonioethanethiosulfonate were determined from the rates of irreversible inhibition of the responses to acetylcholine. The reagents were added in the presence and absence of acetylcholine and at various transmembrane potentials, and the rate constants were extrapolated to zero transmembrane potential. The intrinsic electrostatic potential in the channel in the vicinity of the ring of charge was estimated from the ratios of the rate constants of differently charged reagents. In the acetylcholine-induced open state, this potential was -230 mV with four glutamates in the ring and increased linearly towards 0 mV by +57 mV for each negative charge removed from the ring. Thus, the intrinsic electrostatic potential in the narrow, intracellular end of the open channel is almost entirely due to the intermediate ring of charge and is strongly correlated with alkali-metal-ion conductance through the channel. The intrinsic electrostatic potential in the closed state of the channel was more positive than in the open state at all values of the ring charge. These electrostatic properties were simulated by theoretical calculations based on a simplified model of the channel.

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Year:  2000        PMID: 10653890      PMCID: PMC2217203          DOI: 10.1085/jgp.115.2.93

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  34 in total

1.  Rings of anionic amino acids as structural determinants of ion selectivity in the acetylcholine receptor channel.

Authors:  T Konno; C Busch; E Von Kitzing; K Imoto; F Wang; J Nakai; M Mishina; S Numa; B Sakmann
Journal:  Proc Biol Sci       Date:  1991-05-22       Impact factor: 5.349

Review 2.  Diffusion and kinetic approaches to describe permeation in ionic channels.

Authors:  J A Dani; D G Levitt
Journal:  J Theor Biol       Date:  1990-10-07       Impact factor: 2.691

Review 3.  Surface charges and ion channel function.

Authors:  W N Green; O S Andersen
Journal:  Annu Rev Physiol       Date:  1991       Impact factor: 19.318

4.  A ring of uncharged polar amino acids as a component of channel constriction in the nicotinic acetylcholine receptor.

Authors:  K Imoto; T Konno; J Nakai; F Wang; M Mishina; S Numa
Journal:  FEBS Lett       Date:  1991-09-09       Impact factor: 4.124

5.  Open channel structure and ion binding sites of the nicotinic acetylcholine receptor channel.

Authors:  J A Dani
Journal:  J Neurosci       Date:  1989-03       Impact factor: 6.167

6.  Contribution of the beta subunit M2 segment to the ion-conducting pathway of the acetylcholine receptor.

Authors:  H Zhang; A Karlin
Journal:  Biochemistry       Date:  1998-06-02       Impact factor: 3.162

7.  Location of a threonine residue in the alpha-subunit M2 transmembrane segment that determines the ion flow through the acetylcholine receptor channel.

Authors:  A Villarroel; S Herlitze; M Koenen; B Sakmann
Journal:  Proc Biol Sci       Date:  1991-01-22       Impact factor: 5.349

8.  Electrostatics and the ion selectivity of ligand-gated channels.

Authors:  C Adcock; G R Smith; M S Sansom
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

9.  Acetylcholine receptor channel structure probed in cysteine-substitution mutants.

Authors:  M H Akabas; D A Stauffer; M Xu; A Karlin
Journal:  Science       Date:  1992-10-09       Impact factor: 47.728

10.  Rings of negatively charged amino acids determine the acetylcholine receptor channel conductance.

Authors:  K Imoto; C Busch; B Sakmann; M Mishina; T Konno; J Nakai; H Bujo; Y Mori; K Fukuda; S Numa
Journal:  Nature       Date:  1988-10-13       Impact factor: 49.962

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  30 in total

1.  M2 pore mutations convert the glycine receptor channel from being anion- to cation-selective.

Authors:  A Keramidas; A J Moorhouse; C R French; P R Schofield; P H Barry
Journal:  Biophys J       Date:  2000-07       Impact factor: 4.033

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

3.  Structural basis of open channel block in a prokaryotic pentameric ligand-gated ion channel.

Authors:  Ricarda J C Hilf; Carlo Bertozzi; Iwan Zimmermann; Alwin Reiter; Dirk Trauner; Raimund Dutzler
Journal:  Nat Struct Mol Biol       Date:  2010-10-31       Impact factor: 15.369

4.  Conformational changes of pore helix coupled to gating of TRPV5 by protons.

Authors:  Byung-Il Yeh; Yung Kyu Kim; Wasey Jabbar; Chou-Long Huang
Journal:  EMBO J       Date:  2005-08-25       Impact factor: 11.598

5.  Effects of divalent cations and spermine on the K+ channel TASK-3 and on the outward current in thalamic neurons.

Authors:  Boris Musset; Sven G Meuth; Gong Xin Liu; Christian Derst; Sven Wegner; Hans-Christian Pape; Thomas Budde; Regina Preisig-Müller; Jürgen Daut
Journal:  J Physiol       Date:  2006-05-01       Impact factor: 5.182

6.  Structure of a potentially open state of a proton-activated pentameric ligand-gated ion channel.

Authors:  Ricarda J C Hilf; Raimund Dutzler
Journal:  Nature       Date:  2008-11-05       Impact factor: 49.962

7.  A single ring of charged amino acids at one end of the pore can control ion selectivity in the 5-HT3 receptor.

Authors:  Andrew J Thompson; Sarah C R Lummis
Journal:  Br J Pharmacol       Date:  2003-08-11       Impact factor: 8.739

8.  Accessibility of the CLC-0 pore to charged methanethiosulfonate reagents.

Authors:  Xiao-Dong Zhang; Wei-Ping Yu; Tsung-Yu Chen
Journal:  Biophys J       Date:  2010-02-03       Impact factor: 4.033

9.  Molecular dissection of Cl--selective Cys-loop receptor points to components that are dispensable or essential for channel activity.

Authors:  Dekel D Bar-Lev; Nurit Degani-Katzav; Alexander Perelman; Yoav Paas
Journal:  J Biol Chem       Date:  2011-10-10       Impact factor: 5.157

10.  Conotoxins as sensors of local pH and electrostatic potential in the outer vestibule of the sodium channel.

Authors:  Kwokyin Hui; Deane McIntyre; Robert J French
Journal:  J Gen Physiol       Date:  2003-07       Impact factor: 4.086

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