Desensitization of Mouse Nicotinic Acetylcholine Receptor Channels
Open Access
- 1 August 1998
- journal article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 112 (2), 181-197
- https://doi.org/10.1085/jgp.112.2.181
Abstract
The rate constants of acetylcholine receptor channels (AChR) desensitization and recovery were estimated from the durations and frequencies of clusters of single-channel currents. Diliganded-open AChR desensitize much faster than either unliganded- or diliganded-closed AChR, which indicates that the desensitization rate constant depends on the status of the activation gate rather than the occupancy of the transmitter binding sites. The desensitization rate constant does not change with the nature of the agonist, the membrane potential, the species of permeant cation, channel block by ACh, the subunit composition (ε or γ), or several mutations that are near the transmitter binding sites. The results are discussed in terms of cyclic models of AChR activation, desensitization, and recovery. In particular, a mechanism by which activation and desensitization are mediated by two distinct, but interrelated, gates in the ion permeation pathway is proposed.Keywords
This publication has 43 references indexed in Scilit:
- An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kineticsFEBS Letters, 1996
- Inorganic, monovalent cations compete with agonists for the transmitter binding site of nicotinic acetylcholine receptorsBiophysical Journal, 1996
- Block by acetylcholine of mouse muscle nicotinic receptors, stably expressed in fibroblasts.The Journal of general physiology, 1995
- Modal Shifts in Acetylcholine Receptor Channel Gating Confer Subunit-Dependent DesensitizationScience, 1993
- Nicotinic Acetylcholine Receptor an 9 Å ResolutionJournal of Molecular Biology, 1993
- Postsynaptic potentiation and desensitization at the vertebrate end-plate receptorsProgress in Neurobiology, 1992
- Arrangement of the acetylcholine receptor subunits in the resting and desensitized states, determined by cryoelectron microscopy of crystallized Torpedo postsynaptic membranes.The Journal of cell biology, 1988
- Kinetics of binding of [3H]acetylcholine to Torpedo postsynaptic membranes: association and dissociation rate constants by rapid mixing and ultrafiltrationBiochemistry, 1980
- Single acetylcholine-activated channels show burst-kinetics in presence of desensitizing concentrations of agonistNature, 1980
- Fast Kinetic Studies on the Interaction of a Fluorescent Agonist with the Membrane‐Bound Acetylcholine Receptor from Torpedo marmorataEuropean Journal of Biochemistry, 1979