The synaptic active zone, the site where Ca(2+)-triggered fusion of synaptic vesicles takes place, is commonly associated with protein-rich, electron-dense cytomatrices. The molecular composition and functional role of active zones, especially in the context of vesicular exo- and endocytosis, are under intense investigation. Per se, Drosophila synapses, which display so-called T-bars as electron-dense specializations, should be a highly suitable model system, as they allow for a combination of efficient genetics with ultrastructural and electrophysiological analyses. However, it needed a biochemical approach of the Buchner laboratory to "molecularly" access the T-bar by identification of the CAST/ERC-family member Bruchpilot as the first T-bar-residing protein. Genetic elimination of Bruchpilot revealed that the protein is essential for T-bar formation, calcium channel clustering, and hence proper vesicle fusion and patterned synaptic plasticity. Recently, Bruchpilot was shown to directly shape the T-bar, likely by adopting an elongated conformation. Moreover, first mechanisms that control the availability of Bruchpilot for T-bar assembly were described. This review seeks to summarize the information on T-bar structure, as well as on functional aspects, formulating the hypothesis that T-bars are genuine plasticity modules.
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