Research in Dr. Hughey’s laboratory is focused on characterization of the assembly, processing and membrane trafficking of apically expressed glycoproteins in polarized kidney epithelial cells. She uses biochemistry and electrophysiology techniques to study the function of glycosylation, palmitoylation and proteolytic processing of model proteins such as the epithelial sodium channel (ENaC), gamma-glutamyltranspeptidase and the cell surface sensor MUC1. Her recent studies have revealed that ENaC is activated by a very novel mechanism of proteolytic release of inhibitory peptides in the biosynthetic pathway and post-Golgi compartments, and in pathological states such as proteinuria (kidney) and Cystic Fibrosis (lung). Her current studies of MUC1 function in normal kidney epithelia are focused on its role in epithelial survival and recovery from acute kidney injury.