Nanobinders for Synaptotagmin 1 enable the analysis of synapticvesicle dynamics in rodent and human models.
Goel, R.; Jevdokimenko, K.; Rhem, R.; Hentze, J.; Agui-Gonzalez, P.; Ninov, M.; Lange, F.; Witkowska, A.; Bolz, S.; Pennacchietti, F.; Damenti, M.; Kaempf, N.; Khayenko, V.; Calatayud, C.; Malviya, V. N.; Chanaday, N. L.; Scaletti Hutchinson, E.; Liu, H.; Weyand, K.; Ivanova, D.; Wallis, T.; Small, C.; Maric, H. M.; Joensuu, M.; Cousin, M. A.; Meunier, F. A.; Verstreken, P. A.; Testa, I.; Kavalali, E. T.; Haucke, V.; Jakobs, S.; Urlaub, H.; Brose, N.; Cooper, B. H.; Stenmark, P.; Opazo, F.; Jahn, R.; Rizzoli, S. O.; Fornasiero, E. F.
Show abstract
Synaptic neurotransmission is a critical hallmark of brain activity and one of the first processes to be affected in neural diseases. Monitoring this process, and in particular synaptic vesicle recycling, in living cells has been instrumental in unraveling mechanisms responsible for neurotransmitter release. However, currently available reporters suffer from major limitations such large probe size or lack of suitability for human neurons, hampering the understanding of human synaptic pathophysiology. Here we describe the NbLumSyt1 toolkit, a panel of nanobody-based affinity probes targeting the luminal domain of the synaptic vesicle protein Synaptotagmin 1 (Syt1). These new tools enable quantitative, non-invasive imaging and functional interrogation of synaptic transmission in human neurons, with unprecedented precision, versatility and cost efficiency, in technologies ranging from fixed-and live-cell super-resolution imaging to electron microscopy and mass spectrometry. Overall, NbLumSyt1 nanobinders provide a valuable platform for human synaptic physiology and pathophysiology, benefiting fundamental neuroscience and translational efforts to study and develop treatments for brain-related disorders.
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