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Projekt Druckansicht

Funktionelle Nanoskopie der synaptischen aktiven Zone

Fachliche Zuordnung Molekulare Biologie und Physiologie von Nerven- und Gliazellen
Förderung Förderung von 2015 bis 2020
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 286415047
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

Information processing by the nervous system depends on neurotransmitter release from synaptic vesicles (SVs) at the highly specialized presynaptic active zone (AZ). The precise molecular architecture of AZs gives rise to different structural and functional AZ states, which shape chemical neurotransmission and fundamentally influence brain function. Despite a gradually emerging comprehensive AZ protein catalogue, we still lack basic mechanistic information describing how the nanoscopic organisation and functional interactions of proteins determine AZ physiology. To a large extent, this is due to the diffraction-limited resolution of conventional light microscopy, which has hindered access to the spatial nanodomain in a physiologically relevant context and to experimental difficulties of studying AZ function in vivo. The present research project set out to study how function is encoded in the ultrastructure of AZs. Focusing on Drosophila melanogaster, the experiments took advantage of the powerful tools for manipulating the fruit fly genome and exploited the experimental accessibility of the larval peripheral nervous system. The technology-driven research program focussed on two central work packages. (i) A genetic screen was combined with electrophysiology and superresolution microscopy to characterize molecular mechanisms of AZ plasticity. (ii) New optogenetic approaches were introduced to manipulate synaptic activity in the intact, freely moving organism. The main results identified the conserved SNARE regulator Complexin (Cpx) as a functional interaction partner of the core AZ component Bruchpilot (Brp). Cpx and Brp promote SV recruitment to the filamentous AZ cytomatrix and counteract short-term synaptic depression. Combined with a comparative analysis of mouse ribbon synapses, these findings support an evolutionarily conserved role of Cpx upstream of SNARE complex assembly. In terms of technological advances, highly efficient optogenetic effectors based on Channelrhodopsin-2 derivatives and the photoactivated adenylyl cyclase bPAC were developed. Together with innovative photostimulation strategies, these tools provide new opportunities for studying AZ physiology in a behavioural context.

Projektbezogene Publikationen (Auswahl)

 
 

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