Binding sites contribute unequally to the gating of mouse nicotinic alpha D200N acetylcholine receptors.
- 1 October 1996
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 496 (1) , 185-196
- https://doi.org/10.1113/jphysiol.1996.sp021676
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Estimating single-channel kinetic parameters from idealized patch-clamp data containing missed eventsBiophysical Journal, 1996
- The functional architecture of the acetylcholine nicotinic receptor explored by affinity labelling and site-directed mutagenesisQuarterly Reviews of Biophysics, 1992
- Mutational analysis of ligand-induced activation of the Torpedo acetylcholine receptor.Journal of Biological Chemistry, 1992
- Gamma- and delta-subunits regulate the affinity and the cooperativity of ligand binding to the acetylcholine receptor.Journal of Biological Chemistry, 1991
- Activation of Torpedo acetylcholine receptors expressed in mouse fibroblasts. Single channel current kinetics reveal distinct agonist binding affinities.The Journal of general physiology, 1990
- d-Tubocurarine binding sites are located at alpha-gamma and alpha-delta subunit interfaces of the nicotinic acetylcholine receptor.Proceedings of the National Academy of Sciences, 1990
- Molecular basis of the two nonequivalent ligand binding sites of the muscle nicotinic acetylcholine receptorNeuron, 1989
- Perfection of a synaptic receptor: kinetics and energetics of the acetylcholine receptor.Proceedings of the National Academy of Sciences, 1989
- Single acetylcholine-activated channels show burst-kinetics in presence of desensitizing concentrations of agonistNature, 1980
- A quantitative description of end‐plate currentsThe Journal of Physiology, 1972