, 2005), Pannexin-2, a large pore ion channel expressed in the brain (MacVicar and Thompson, 2010), and Rab11fip5, which regulates the small GTPase Rab11 involved in membrane recycling (Horgan and McCaffrey, 2009). Given their high sequence homology, especially in the kinase domain, and indistinguishable biochemical properties as so-far tested, taken together with the ability of NDR1 to rescue for NDR1/2 reduction, NDR1 and NDR2 probably have common substrates. We were particularly interested in the two most prevalent candidates AAK1 and Rabin8, because both function in intracellular vesicle trafficking. AAK1 Selleck Tenofovir was identified

in seven out of eight experiments, and Rabin8 was identified in three out of eight experiments. Moreover, the yeast Rabin8 homolog Sec2p is phosphorylated by the yeast NDR kinase Cbk1p (Kurischko et al., 2008), indicating that this kinase regulation might be evolutionarily conserved. We confirmed that AAK1 and Rabin8 were indeed phosphorylated by NDR1 by using direct kinase assay (Figures 5E and 5F). We reacted purified NDR1-as-CA with purified substrate proteins using Benzyl-ATP-γ-S and detected phosphorylation by antithiophosphate ester antibody after esterification with PNBM (Figures 5E and 5F), a method that avoids the background caused by

AAK1 autophosphorylation when OSI-744 nmr using radioactive ATP for detection. We confirmed that the AAK1 phosphorylation site was indeed S635, as was identified

in mass spectrometry (Figure 5G), since S635A mutant was not phosphorylated (Figure 5E). Furthermore, we generated an antibody that targets AAK1 phosphorylated at S635 (anti-AAK1 P-S635). When coexpressed in COS-7 cells, NDR1-CA specifically phosphorylated S635 of AAK1 in intact cells (Figure S5E). However, it should be noted that this antibody did not exclusively stain the endogenous phosphorylated AAK1 by immunocytochemistry (data not shown). Rabin8 was phosphorylated by NDR1 at S240 (Figure S4D). We also showed that wild-type NDR1 (activated by okadaic acid) and NDR1-CA could phosphorylate Rabin8 at S240 using ATP-γ-S (Figure S4C). However, there are likely other residues that can be phosphorylated, because the S240A mutant L-NAME HCl could be still phosphorylated albeit at a reduced level (Figure 5F). Interestingly, Rabin8 S240 was followed by a stretch of T241, S242, and S243. When all S/T240- 243 were mutated to Ala, NDR1 no longer phosphorylated Rabin8 (Figure 5F). Next, we investigated the function of AAK1 on dendrite and spine development. In cultured hippocampal neurons, AAK1 is in the cytoplasm, dendrites, and axons but is excluded from the nucleus as shown by immunostaining of endogeneous AAK1 by the anti-AAK1 antibody (Figure S5C).