Journal of Biological Chemistry · 2007 · 46 citations · 35 references
Natural SciencesBiophysicsMolecular BiologyMolecular BiophysicsMolecular Cell BiologyMolecular ImagingChannel StructureCystic FibrosisIon Channel DisordersIon Channel PhysiologyIon ChannelsSodium Channel BiophysicsCftr Protein FunctionChloride Channel PhysiologyEpithelial Sodium ChannelsFluorescence Resonance Energy TransferIon Channel LocalizationIon Channel Structure-function RelationshipsMolecular Fluorescence ImagingSodium Channel Physiology
We present the evidence for a direct physical association of cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial sodium channel (ENaC), two major ion channels implicated in the pathophysiology of cystic fibrosis, a devastating inherited disease. We employed fluorescence resonance energy transfer, a distance-dependent imaging technique with capability to detect molecular complexes with near angstrom resolution, to estimate the proximity of CFTR and ENaC, an essential variable for possible physical interaction to occur. Fluorescence resonance energy transfer studies were complemented with a classic biochemical approach: coimmunoprecipitation. Our results place CFTR and ENaC within reach of each other, suggestive of a direct interaction between these two proteins.
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