University of Toronto biologists leading an investigation into the cells that regulate proper brain function identified and located the key players whose actions contribute to afflictions such as epilepsy and schizophrenia.
"Neurons in the brain communicate with other neurons through synapses, communication that can either excite or inhibit other neurons," said Professor Melanie Woodin in the Department of Cell and Systems Biology at U of T, and lead investigator of the study.
"We identified a key complex of proteins that can regulate excitation-inhibition balance at the cellular level," Woodin said.
This complex brings together three key proteins required for inhibitory and excitatory synaptic communication. The protein KCC2 is required for inhibitory impulses, while GluK2 is a receptor for the main excitatory transmitter glutamate, and Neto2 is an auxiliary protein that interacts with the other two proteins.
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The discovery of the complex of three proteins is pathbreaking as it was previously believed that KCC2 and GluK2 were in separate compartments of the cell and acted independently of each other.
Mahadevan and fellow researchers made the discovery via biochemistry, fluorescence imaging and electrophysiology experiments on mice brains.
The most fruitful technique was the application of an advanced sensitive gel system to determine native protein complexes in neurons, called Blue Native PAGE.
The process provided the biochemical conditions necessary to preserve the protein complexes that normally exist in neurons.
"There is no cure for epilepsy; the best available treatments only control its effects, such as convulsions and seizures. We can now imagine preventing them from occurring in the first place," Woodin said.
The findings are reported in the journal Cell Reports.