Cargando…
Openings of the Rat Recombinant α1 Homomeric Glycine Receptor as a Function of the Number of Agonist Molecules Bound
The functional properties of rat homomeric α1 glycine receptors were investigated using whole-cell and outside-out recording from human embryonic kidney cells transfected with rat α1 subunit cDNA. Whole-cell dose-response curves gave EC (50) estimates between 30 and 120 μM and a Hill slope of ∼3.3....
Autores principales: | Beato, Marco, Groot-Kormelink, Paul J., Colquhoun, David, Sivilotti, Lucia G. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2002
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233816/ https://www.ncbi.nlm.nih.gov/pubmed/11981023 http://dx.doi.org/10.1085/jgp.20028530 |
Ejemplares similares
-
The intracellular domain of homomeric glycine receptors modulates agonist efficacy
por: Ivica, Josip, et al.
Publicado: (2021) -
The kinetics of inhibition of rat recombinant heteromeric α1β glycine receptors by the low-affinity antagonist SR-95531
por: Beato, Marco, et al.
Publicado: (2007) -
Acidic pH reduces agonist efficacy and responses to synaptic‐like glycine applications in zebrafish α1 and rat α1β recombinant glycine receptors
por: Ivica, Josip, et al.
Publicado: (2021) -
The Startle Disease Mutation E103K Impairs Activation of Human Homomeric α1 Glycine Receptors by Disrupting an Intersubunit Salt Bridge across the Agonist Binding Site
por: Safar, Fatemah, et al.
Publicado: (2017) -
Single-channel properties of glycine receptors of juvenile rat spinal motoneurones in vitro
por: Beato, Marco, et al.
Publicado: (2007)