Lucia Sivilotti | University College London (original) (raw)
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Papers by Lucia Sivilotti
The Journal of Physiology, Apr 1, 1997
The Journal of Physiology, Jun 18, 2020
The Journal of Physiology, Feb 1, 1998
The Journal of Physiology, Nov 15, 1994
The Journal of Physiology, Oct 30, 2009
The Journal of Neuroscience, Dec 1, 2004
The Journal of General Physiology, Jan 31, 2011
The Journal of Physiology, May 4, 2007
The Journal of Neuroscience, Jan 25, 2012
Biophysical Journal, Feb 1, 2009
The Journal of General Physiology, Dec 29, 2014
Biophysical Journal, 2010
Biophysical Journal, Feb 1, 2011
The Journal of Physiology, 2021
Journal of Biological Chemistry, 2020
Like other pentameric ligand-gated channels, glycine receptors (GlyRs) contain long intracellular... more Like other pentameric ligand-gated channels, glycine receptors (GlyRs) contain long intracellular domains (ICDs) between transmembrane helices 3 and 4. Structurally characterized GlyRs are generally engineered to have a very short ICD. We show here that for one such construct, zebrafish GlyREM, the agonists glycine, β-alanine, taurine, and GABA have high efficacy and produce maximum single-channel open probabilities greater than 0.9. In contrast, for full-length human α1 GlyR, taurine and GABA were clearly partial agonists, with maximum open probabilities of 0.46 and 0.09, respectively. We found that the elevated open probabilities in GlyREM are not due to the limited sequence differences between the human and zebrafish orthologs, but rather to replacement of the native ICD with a short tripeptide ICD. Consistent with this interpretation, shortening the ICD in the human GlyR increased the maximum open probability produced by taurine and GABA to 0.90 and 0.70, respectively, but furth...
The Journal of Physiology, Apr 1, 1997
The Journal of Physiology, Jun 18, 2020
The Journal of Physiology, Feb 1, 1998
The Journal of Physiology, Nov 15, 1994
The Journal of Physiology, Oct 30, 2009
The Journal of Neuroscience, Dec 1, 2004
The Journal of General Physiology, Jan 31, 2011
The Journal of Physiology, May 4, 2007
The Journal of Neuroscience, Jan 25, 2012
Biophysical Journal, Feb 1, 2009
The Journal of General Physiology, Dec 29, 2014
Biophysical Journal, 2010
Biophysical Journal, Feb 1, 2011
The Journal of Physiology, 2021
Journal of Biological Chemistry, 2020
Like other pentameric ligand-gated channels, glycine receptors (GlyRs) contain long intracellular... more Like other pentameric ligand-gated channels, glycine receptors (GlyRs) contain long intracellular domains (ICDs) between transmembrane helices 3 and 4. Structurally characterized GlyRs are generally engineered to have a very short ICD. We show here that for one such construct, zebrafish GlyREM, the agonists glycine, β-alanine, taurine, and GABA have high efficacy and produce maximum single-channel open probabilities greater than 0.9. In contrast, for full-length human α1 GlyR, taurine and GABA were clearly partial agonists, with maximum open probabilities of 0.46 and 0.09, respectively. We found that the elevated open probabilities in GlyREM are not due to the limited sequence differences between the human and zebrafish orthologs, but rather to replacement of the native ICD with a short tripeptide ICD. Consistent with this interpretation, shortening the ICD in the human GlyR increased the maximum open probability produced by taurine and GABA to 0.90 and 0.70, respectively, but furth...