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Project C12, led by Eugenio F. Fornasiero (University Medical Center Göttingen) and Johanna Senk (Forschungszentrum Jülich), are developing a multiscale computational model of synaptic turnover to understand how dynamic molecular renewal shapes synaptic function. Synapses constantly replace proteins, mRNAs, and post-translational modifications across spatial and temporal scales, yet how their molecular renewal sustains stability and plasticity remains unclear.

Building on extensive quantitative datasets the project will integrate experimental and theoretical approaches in iterative cycles. Special will be given to aging, which slows molecular renewal and impairs synaptic resilience. The resulting framework will identify functional bottlenecks, clarify principles of synaptic adaptability, and improve models of synaptic plasticity and age-related dysfunction.

Eugenio Fornasiero

Principal Investigators

Johanna Senk

Principal Investigators
More subprojects

A5:“Mitochondrial heterogeneity in synapses”

Stefan Jakobs

A11: “Regulation of synaptic functional heterogeneity and diversity”

Noa Lipstein

B11 “Gating and expression of long-term synaptic plasticity as an interplay between parallel transmission sites and astrocyte signalling”

Oliver M. Schlüter