There is little information about the mechanisms by which G-protein–coupled receptors gate ion channels although many ionotropic receptors are well studied. We have investigated gating of the muscarinic cationic channel, which mediates the excitatory effect of acetylcholine in smooth muscles, and proposed a scheme consisting of four pairs of closed and open states. Channel kinetics appeared to be the same in cell-attached or outside-out patches whether the channel was activated by carbachol application or by intracellular dialysis with GTPγS. Since in the latter case G-proteins are permanently active, it is concluded that the cationic channel is the major determinant of its own gating, similarly to the KACh channel (Ivanova-Nikolova, T.T., and G.E. Breitwieser. 1997. J. Gen. Physiol. 109:245–253). Analysis of adjacent-state dwell times revealed connections between the states that showed features conserved among many other ligand-gated ion channels (e.g., nAChR, BKCa channel). Open probability (PO) of the cationic channel was increased by membrane depolarization consistent with the prominent U-shaped I-V relationship of the muscarinic whole-cell current at negative potentials. Membrane potential affected transitions within each closed-open state pair but had little effect on transitions between pairs; thus, the latter are likely to be caused by interactions of the channel with its ligands, e.g., Ca2+ and Gαo-GTP. Channel activity was highly heterogeneous, as was evident from the prominent cycling behavior when PO was measured over 5-s intervals. This was related to the variable frequency of openings (as in the KACh channel) and, especially, to the number of long openings between consecutive long shuttings. Analysis of the underlying Markov chain in terms of probabilities allowed us to evaluate the contribution of each open state to the integral current (from shortest to longest open state: 0.1, 3, 24, and 73%) as PO increased 525-fold in three stages.
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1 May 2004
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April 26 2004
G-protein–gated TRP-like Cationic Channel Activated by Muscarinic Receptors : Effect of Potential on Single-channel Gating
Alexander V. Zholos,
Alexander V. Zholos
1Laboratory of Molecular Pharmacology of Cellular Receptors and Ion Channels, A.A. Bogomoletz Institute of Physiology, Kiev, 01024 Ukraine
3Pharmacology and Clinical Pharmacology Basic Medical Sciences, St. George's Hospital Medical School, London SW17 ORE, UK
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Andrey A. Zholos,
Andrey A. Zholos
2Department of Economical Cybernetics, Taras Shevchenko National University, Kiev, 01033 Ukraine
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Thomas B. Bolton
Thomas B. Bolton
3Pharmacology and Clinical Pharmacology Basic Medical Sciences, St. George's Hospital Medical School, London SW17 ORE, UK
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Alexander V. Zholos
1Laboratory of Molecular Pharmacology of Cellular Receptors and Ion Channels, A.A. Bogomoletz Institute of Physiology, Kiev, 01024 Ukraine
3Pharmacology and Clinical Pharmacology Basic Medical Sciences, St. George's Hospital Medical School, London SW17 ORE, UK
Andrey A. Zholos
2Department of Economical Cybernetics, Taras Shevchenko National University, Kiev, 01033 Ukraine
Thomas B. Bolton
3Pharmacology and Clinical Pharmacology Basic Medical Sciences, St. George's Hospital Medical School, London SW17 ORE, UK
Address correspondence to Alexander V. Zholos, Laboratory of Molecular Pharmacology of Cellular Receptors and Ion Channels, A.A. Bogomoletz Institute of Physiology, Kiev, 01024 Ukraine. Fax: (044) 256 2000; email: [email protected]
Abbreviations used in this paper: ACh, acetylcholine; GPCR, G-protein–coupled receptor; mAChR, muscarinic receptor; nAChR, nicotinic acetylcholine receptor; TRP, transient receptor potential.
Received:
December 22 2003
Accepted:
March 29 2004
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2004
J Gen Physiol (2004) 123 (5): 581–598.
Article history
Received:
December 22 2003
Accepted:
March 29 2004
Citation
Alexander V. Zholos, Andrey A. Zholos, Thomas B. Bolton; G-protein–gated TRP-like Cationic Channel Activated by Muscarinic Receptors : Effect of Potential on Single-channel Gating . J Gen Physiol 1 May 2004; 123 (5): 581–598. doi: https://doi.org/10.1085/jgp.200309002
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