We have formulated the following objectives:

  1. To provide a quantitative description of protein complexes, interactomes and networks in the mammalian glutamatergic synapse.
  2. To generate quantitative dynamic models, describing the main functional features of the synaptic networks.
  3. To reiterate on modeling by relating model predictions to synaptic function.
  4. To identify vulnerabilities in gene networks that are at the basis of human brain disease and may help design future therapy.

4th European Synapse Meeting

28 - 30 August 2013
Bordeaux, France