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Membrane Biology
2 Results
- Membrane BiologyOpen Access
Specific Palmitoyltransferases Associate with and Activate the Epithelial Sodium Channel
Journal of Biological ChemistryVol. 292Issue 10p4152–4163Published online: January 30, 2017- Anindit Mukherjee
- Zhijian Wang
- Carol L. Kinlough
- Paul A. Poland
- Allison L. Marciszyn
- Nicolas Montalbetti
- and others
Cited in Scopus: 14The epithelial sodium channel (ENaC) has an important role in regulating extracellular fluid volume and blood pressure, as well as airway surface liquid volume and mucociliary clearance. ENaC is a trimer of three homologous subunits (α, β, and γ). We previously reported that cytoplasmic residues on the β (βCys-43 and βCys-557) and γ (γCys-33 and γCys-41) subunits are palmitoylated. Mutation of Cys that blocked ENaC palmitoylation also reduced channel open probability. Furthermore, γ subunit palmitoylation had a dominant role over β subunit palmitoylation in regulating ENaC. - Membrane BiologyOpen Access
Functional Roles of Clusters of Hydrophobic and Polar Residues in the Epithelial Na+ Channel Knuckle Domain
Journal of Biological ChemistryVol. 290Issue 41p25140–25150Published online: August 25, 2015- Jingxin Chen
- Evan C. Ray
- Megan E. Yates
- Teresa M. Buck
- Jeffrey L. Brodsky
- Carol L. Kinlough
- and others
Cited in Scopus: 10Background: There are regulatory interactions between ENaC and extracellular factors.Results: Mutations of multiple α subunit knuckle residues activate ENaC by suppressing the inhibitory effect of Na+. Channels lacking the β or γ subunit knuckle have processing defects.Conclusion: Interactions between the α subunit knuckle and palm/finger domains regulate ENaC.Significance: Intrasubunit domain-domain interactions have important regulatory roles.