, 2006). Strikingly, a deletion of the 17 C-terminal residues of bruchpilot (which are part of the plectin-homology region) impaired attachment of synaptic vesicles to t bars in Drosophila synapses and altered synaptic transmission, suggesting that a major contribution to bruchpilot function is derived from the plectin-homology check details region ( Hallermann et al., 2010). Overall, these studies suggest that bruchpilot performs a double function in Drosophila

synapses, with the N-terminal ELKS component acting like a standard ELKS protein, and the C-terminal plectin-homology region acting in vesicle recruitment analogous to piccolo and bassoon in mammalian synapses (see below). Primarily due to pioneering work by the Gundelfinger laboratory, piccolo and bassoon are among the best studied presynaptic proteins. Piccolo and bassoon are large proteins specific to vertebrates Alectinib cell line whose major function appears to be to guide synaptic vesicles from the backfield of the synapse to the active zone (Mukherjee et al., 2010 and Hallermann et al., 2010). Most piccolo and bassoon sequences are homologous and are predicted to form N-terminal zinc finger domains followed by extended coiled-coil structures without clear domain boundaries (tom Dieck et al., 1998 and Wang

et al., 1999). Moreover, piccolo contains a C-terminal PDZ domain and two C2 domains. Different from other C2 domains, the first C2 domain of piccolo undergoes a major conformational change upon Ca2+ binding,

while the second C2 domain does not bind Ca2+ but is alternatively spliced (Wang et al., 1999, Gerber et al., 2001 and Garcia et al., 2004). Partial knockout of bassoon causes partial lethality and impairs neurotransmitter release (Altrock et al., 2003), whereas deletion of piccolo has no significant effect on survival or on neurotransmitter release in cultured neurons or in acute slices (Mukherjee et al., 2010). In synapses with a partial loss of both piccolo and bassoon, synaptic vesicle clusters are disrupted, indicating a possible role for these proteins in vesicle clustering (Mukherjee et al., 2010). Ketanserin Given the size of piccolo and bassoon, the interesting C-terminal domains of piccolo, and the reactive changes observed in bassoon knockout mice (Heyden et al., 2011), it seems likely that the more peripheral active zone function of piccolo and bassoon will have an important role in overall brain performance. This role may be particularly important in specialized synapses such as hippocampal mossy fiber synapses or retinal ribbon synapses. Among the problems in characterizing this role, however, has been the difficulty in generating conditional knockouts and the large size of the proteins which makes biochemical studies nearly impossible. CASK is composed of an N-terminal CaM kinase-like domain that constitutes a catalytically active, unusual protein kinase (Mukherjee et al.