Abstract
Apical expression of the large-conductance, calcium- and voltage-activated potassium (MaxiK) channel in the cortical collecting duct is responsible for flow-stimulated potassium secretion. Here, we identify two cytoplasmic regions controlling apical expression of the MaxiK channel. Disruption of the proximal region results in the intracellular retention of the MaxiK channel without affecting channel assembly, thereby reducing surface expression. Coexpression of the WT channel with this mutant results in a reduction of WT MaxiK channel at the cell surface. Our data indicate that this proximal region is necessary for export of the MaxiK channel from the endoplasmic reticulum as a way to assess the final assembly of the channel. Deletion of a more distal region disrupts apical sorting, resulting in a nonpolarized distribution of the channel without impairing its surface delivery. In summary, we have found that sequences of amino acids in the C terminus of the MaxiK channel operate after the channel is assembled into a multimer and play a role in its expression, movement to the cell surface, and apical localization.
MeSH Terms
Animals
Biological Transport, Active
COS Cells
Cell Membrane/metabolism
Cytoplasm/metabolism
Endoplasmic Reticulum/metabolism
Gene Expression
Large-Conductance Calcium-Activated Potassium Channels
Mutation
Potassium Channels, Calcium-Activated/chemistry,genetics,metabolism
Protein Structure, Quaternary
Recombinant Proteins/chemistry,genetics,metabolism
Sequence Deletion
Transfection
Chemicals
Large-Conductance Calcium-Activated Potassium Channels
Potassium Channels, Calcium-Activated
Recombinant Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kwon Sang-Ho
Department of Physiology, School of Medicine, The Johns Hopkins University, Baltimore, MD 21205, USA.
Guggino William B
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