Dinudom, A.Harvey, K.Komwatanat, P.Jolliffe, C.Young, J.Kumar, S.Cook, D.2006-06-262006-06-262001Journal of Biological Chemistry, 2001; 276(17):13744-137490021-92581083-351Xhttp://hdl.handle.net/2440/9554The amiloride-sensitive epithelial Na+ channels (ENaC) in the intralobular duct cells of mouse mandibular glands are inhibited by the ubiquitin-protein ligase, Nedd4, which is activated by increased intracellular Na+. In this study we have used whole-cell patch clamp methods in mouse mandibular duct cells to investigate the role of the C termini of the α-, β-, and γ-subunits of ENaC in mediating this inhibition. We found that peptides corresponding to the C termini of the β- and γ-subunits, but not the α-subunit, inhibited the activity of the Na+ channels. This mechanism did not involve Nedd4 and probably resulted from the exogenous C termini interfering competitively with the protein-protein interactions that keep the channels active. In the case of the C terminus of mouse β-ENaC, the interacting motif included βSer631, βAsp632, and βSer633. In the C terminus of mouse γ-ENaC, it included γSer640. Once these motifs were deleted, we were able to use the C termini of β- and γ-ENaC to prevent Nedd4-mediated down-regulation of Na+ channel activity. The C terminus of the α-subunit, on the contrary, did not prevent Nedd4-mediated inhibition of the Na+ channels. We conclude that mouse Nedd4 interacts with the β- and γ-subunits of ENaC.en© 2001 by The American Society for Biochemistry and Molecular Biology, Inc.MandibleCytosolAnimalsMiceSodiumAmilorideGlutathione TransferasePeptidesSodium ChannelsRecombinant Fusion ProteinsDNA, ComplementaryVirulence Factors, BordetellaPatch-Clamp TechniquesAmino Acid SequenceAmino Acid MotifsProtein Structure, TertiarySequence Homology, Amino AcidPhosphorylationDose-Response Relationship, DrugPlasmidsMolecular Sequence DataEpithelial Sodium ChannelsJournal article002001107810.1074/jbc.M0112732000001683566000342-s2.0-003595798261595Kumar, S. [0000-0001-7126-9814]