|
||
Article |
Address correspondence to Peter H. Barry, Department of Physiology and Pharmacology, University of New South Wales, Sydney 2052, Australia. Tel.: (61) 2-9385-1101; Fax: 61-2-9385-1099; E-mail: p.barry{at}unsw.edu.au
Members of the ligand-gated ion channel superfamily mediate fast synaptic transmission in the nervous system. In this study, we investigate the molecular determinants and mechanisms of ion permeation and ion charge selectivity in this family of channels by characterizing the single channel conductance and rectification of
1 homomeric human glycine receptor channels (GlyRs) containing pore mutations that impart cation selectivity. The A-1'E mutant GlyR and the selectivity double mutant ([SDM], A-1'E, P-2'
) GlyR, had mean inward chord conductances (at -60 mV) of 7 pS and mean outward conductances of 11 and 12 pS (60 mV), respectively. This indicates that the mutations have not simply reduced anion permeability, but have replaced the previous anion conductance with a cation one. An additional mutation to neutralize the ring of positive charge at the extracellular mouth of the channel (SDM+R19'A GlyR) made the conductancevoltage relationship linear (14 pS at both 60 and -60 mV). When this external charged ring was made negative (SDM+R19'E GlyR), the inward conductance was further increased (to 22 pS) and now became sensitive to external divalent cations (being 32 pS in their absence). The effects of the mutations to the external ring of charge on conductance and rectification could be fit to a model where only the main external energy barrier height for permeation was changed. Mean outward conductances in the SDM+R19'A and SDM+R19'E GlyRs were increased when internal divalent cations were absent, consistent with the intracellular end of the pore being flanked by fixed negative charges. This supports our hypothesis that the ion charge selectivity mutations have inverted the electrostatic profile of the pore by introducing a negatively charged ring at the putative selectivity filter. These results also further confirm the role of external pore vestibule electrostatics in determining the conductance and rectification properties of the ligand-gated ion channels.
Key Words: ligand-gated ion channels rings of charge ion permeation ion selectivity M2 domain
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
J. E. Carland, M. A. Cooper, S. Sugiharto, H.-J. Jeong, T. M. Lewis, P. H. Barry, J. A. Peters, J. J. Lambert, and A. J. Moorhouse Characterization of the Effects of Charged Residues in the Intracellular Loop on Ion Permeation in {alpha}1 Glycine Receptor Channels J. Biol. Chem., January 23, 2009; 284(4): 2023 - 2030. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. N. St. Aubin and P. Linsdell Positive Charges at the Intracellular Mouth of the Pore Regulate Anion Conduction in the CFTR Chloride Channel J. Gen. Physiol., November 1, 2006; 128(5): 535 - 545. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Sunesen, L. P. de Carvalho, V. Dufresne, R. Grailhe, N. Savatier-Duclert, G. Gibor, A. Peretz, B. Attali, J.-P. Changeux, and Y. Paas Mechanism of Cl- Selection by a Glutamate-gated Chloride (GluCl) Receptor Revealed through Mutations in the Selectivity Filter J. Biol. Chem., May 26, 2006; 281(21): 14875 - 14881. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Qu, A. J. Moorhouse, M. Chandra, K. D. Pierce, T. M. Lewis, and P. H. Barry A Single P-loop Glutamate Point Mutation to either Lysine or Arginine Switches the Cation-Anion Selectivity of the CNGA2 Channel J. Gen. Physiol., March 27, 2006; 127(4): 375 - 389. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Johnson Jr. and W. N. Zagotta The carboxyl-terminal region of cyclic nucleotide-modulated channels is a gating ring, not a permeation path PNAS, February 22, 2005; 102(8): 2742 - 2747. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Carland, A. J. Moorhouse, P. H. Barry, G. A. R. Johnston, and M. Chebib Charged Residues at the 2' Position of Human GABAC {rho}1 Receptors Invert Ion Selectivity and Influence Open State Probability J. Biol. Chem., December 24, 2004; 279(52): 54153 - 54160. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. Lynch Molecular Structure and Function of the Glycine Receptor Chloride Channel Physiol Rev, October 1, 2004; 84(4): 1051 - 1095. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. O'Mara, P. H. Barry, and S.-H. Chung A model of the glycine receptor deduced from Brownian dynamics studies PNAS, April 1, 2003; 100(7): 4310 - 4315. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Keramidas, A. J. Moorhouse, K. D. Pierce, P. R. Schofield, and P. H. Barry Cation-selective Mutations in the M2 Domain of the Inhibitory Glycine Receptor Channel Reveal Determinants of Ion-Charge Selectivity J. Gen. Physiol., May 1, 2002; 119(5): 393 - 410. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Keramidas, A. J. Moorhouse, K. D. Pierce, P. R. Schofield, and P. H. Barry Cation-selective Mutations in the M2 Domain of the Inhibitory Glycine Receptor Channel Reveal Determinants of Ion-Charge Selectivity J. Gen. Physiol., May 1, 2002; 119(5): 393 - 410. [Abstract] [Full Text] [PDF] |
||||
|
|