Pain & migraine
How TREK/TRESK K2P assemblies set nociceptor excitability, and how they can be modulated — from a bacterial analgesic toxin to photoswitchable channel inhibitors that control pain in freely moving animals.
Institut de Biologie Valrose · Nice, France
We explore the ion channels that shape neuronal activity — and develop optical tools to understand how they change in disease and control their activity precisely when and where needed, taking advantage of the exceptional spatial resolution provided by a beam of light.
Selected journals
CellNeuronNature CommunicationsPNASEMBO Journal
01 / Our research
Two-pore-domain potassium (K2P) channels help set the resting potential and firing threshold of neurons. We study how these molecular gatekeepers work, how they change in disease, and how light can control their activity precisely when and where needed.
How TREK/TRESK K2P assemblies set nociceptor excitability, and how they can be modulated — from a bacterial analgesic toxin to photoswitchable channel inhibitors that control pain in freely moving animals.
TRESK-dependent shunting inhibition and alternative translation initiation as mechanisms linking specific K2P mutations to neuronal hyperexcitability and seizure susceptibility.
Defining native K2P homo- and heteromeric assemblies with single-molecule pulldown, and how auxiliary subunits and lipid signalling reshape channel composition and function.
Molecular discovery · Cell, 2021
KCNE1 bridges two unrelated ion channel superfamilies, inducing a voltage-dependent current in the calcium-activated chloride channel TMEM16A.
Explore the paperTranslational programme · Ionic
The Ionic project extends our ion-channel work toward precise, reversible ways to understand and modulate excitability — connecting the molecular insight from our Cell study on TMEM16A to future applications.
Research in action
02 / How we work
Optical tools, electrophysiology and single-molecule imaging connect channel mechanisms to neuronal activity and behaviour.
03 / Publications
Our work appears in Cell, Neuron, Nature Communications, PNAS and EMBO Journal, with studies highlighted in journal commentaries and recognized by the scientific community.
60 peer-reviewed publications · Selected articles below
Selected papers below are led by the G. Sandoz Lab, with the team represented among the corresponding authors — including work in Cell and Neuron, three PNAS papers and three Nature Communications papers.
Nature Communications 17:620
Nature Communications 15(1):65
Nature Communications 14(1):1160
Neuroscience Letters 773:136494
Current Opinion in Pharmacology 63:102178
Cell 184(2):534–544
iScience 24(9):102961
The Neuroscientist 27(3):268–284
Neuron 101(2):232–245 — recommended by F1000, highlighted in Neuron
Neuron 104(5):831–833
PNAS 106:14628–14633 — Editors' choice, Science Signaling
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See the full list on PubMed
04 / Our people
Our team brings together ion channel biophysics, chemical biology, single-molecule imaging and behaviour at the Institut de Biologie Valrose in Nice.