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Full-Text Articles in Biotechnology
Mutational Analysis Of The Rotavirus Nsp4 Enterotoxic Domain That Binds To Caveolin-1, Judith M. Ball, Megan E. Schroeder, Cecelia V. Williams, Friedhelm Schroeder, Rebecca D. Parr
Mutational Analysis Of The Rotavirus Nsp4 Enterotoxic Domain That Binds To Caveolin-1, Judith M. Ball, Megan E. Schroeder, Cecelia V. Williams, Friedhelm Schroeder, Rebecca D. Parr
Faculty Publications
Background: Rotavirus (RV) nonstructural protein 4 (NSP4) is the first described viral enterotoxin, which induces early secretory diarrhea in neonatal rodents. Our previous data show a direct interaction between RV NSP4 and the structural protein of caveolae, caveolin-1 (cav-1), in yeast and mammalian cells. The binding site of cav-1 mapped to the NSP4 amphipathic helix, and led us to examine which helical face was responsible for the interaction.
Methods: A panel of NSP4 mutants were prepared and tested for binding to cav-1 by yeast two hybrid and direct binding assays. The charged residues of the NSP4 amphipathic helix were changed …
Rotavirus Nsp4: Cell Type-Dependent Transport Kinetics To The Exofacial Plasma Membrane And Release From Intact Infected Cells, Thomas F. Gibbons, Stephen M. Storey, Cecelia V. Williams, Avery Mcintosh, Deanne M. Mitchel, Rebecca D. Parr, Friedhelm Schroeder, Judith M. Ball
Rotavirus Nsp4: Cell Type-Dependent Transport Kinetics To The Exofacial Plasma Membrane And Release From Intact Infected Cells, Thomas F. Gibbons, Stephen M. Storey, Cecelia V. Williams, Avery Mcintosh, Deanne M. Mitchel, Rebecca D. Parr, Friedhelm Schroeder, Judith M. Ball
Faculty Publications
Background
Rotavirus NSP4 localizes to multiple intracellular sites and is multifunctional, contributing to RV morphogenesis, replication and pathogenesis. One function of NSP4 is the induction of early secretory diarrhea by binding surface receptors to initiate signaling events. The aims of this study were to determine the transport kinetics of NSP4 to the exofacial plasma membrane (PM), the subsequent release from intact infected cells, and rebinding to naïve and/or neighboring cells in two cell types.
Methods
Transport kinetics was evaluated using surface-specific biotinylation/streptavidin pull-downs and exofacial exposure of NSP4 was confirmed by antibody binding to intact cells, and fluorescent resonant energy …