, 2011). In addition, it should be noted that the presented AMPAR proteome relies on the sensitivity and dynamic range of our MS analyses. Thus, proteins interacting with the AMPAR complexes at high dynamics or proteins with very low or highly select expression (resulting in protein Selleckchem Kinase Inhibitor Library amounts < 0.1 femtomole) may have escaped detection (Bildl et al., 2012 and Müller et al., 2010). About half of the newly identified AMPAR constituents lack any annotation of primary function(s) in public databases and scientific literature, while others have not yet been investigated for

their role in AMPAR function. Thus, the results obtained with the not yet annotated GSG1-l protein are significant in two aspects: first, they assign GSG1-l the role of an inner core constituent modifying the gating of AMPARs similar to the other known auxiliary

subunits (Figure 2, Figure 3, Figure 4 and Figure 5). Second, they demonstrate the distinct functional consequences generated by coassembly of different types of auxiliary subunits into the same AMPAR (Figure 5). This observation emphasizes the general importance of heteromultimeric assemblies, as observed with most AMPARs in the brain (Figures 2 and 3), and indicates that AMPAR functions beyond ligand-driven channel gating may be largely determined by their non-GluA constituents. For a few of the AMPAR constituents identified here, see more databases and literature offer some striking links toward AMPAR function and physiology. Thus, the membrane-anchored Neuritin, originally identified as cpg15 in a screen for plasticity-related genes in the hippocampus ( Nedivi et al., 1993), was shown to promote maturation of synapses supposedly by recruiting AMPARs to the postsynapse ( Cantallops et al., 2000). Similar roles may be expected for LRRT4, a member of the

LRRTM family of proteins recently shown to promote formation of excitatory synapses ( Ko et al., Resveratrol 2009 and Linhoff et al., 2009), or for PRRTs 1,2 that are structurally related to SynDIG1, a protein involved in the development of excitatory synapses ( Kalashnikova et al., 2010). Finally, CPT-1 and PORCN are TM proteins with enzymatic activities involved in palmitoylation of cysteine residues, a posttranslational modification that was shown to occur on all GluAs and to modulate receptor trafficking ( Hayashi et al., 2005); similarly, modulation of AMPAR trafficking related to synaptic plasticity has been reported for the small GTP-binding protein Rap-2b ( Hussain et al., 2010 and Zhu et al., 2002). In conclusion, the AMPAR proteome as presented here defines the molecular framework for the complex cell physiology of AMPARs in excitatory synaptic transmission and provides a roadmap for further in-depth structural and functional investigations. Preparation and injection of cRNAs into Xenopus oocytes were done as described ( Fakler et al., 1995). All cDNAs were verified by sequencing; GenBank accession numbers of the clones used are as follows: M38060.