Abstract
The binding of interferons-α (IFN-α) to various cells is well characterized,but fewer studies have reported on the interaction of IFN-α with receptors on plasma membranes or in detergent-solubilized form. We describe a simple, sensitive, and semiquantitative assay procedure to detect the presence of IFN-α receptors on bovine spleen plasma membrane preparations or in detergent-solubilized extracts. The procedure involves spotting the sample on hydrophobic polyvinylidene difluoride (PVDF; Immobilon P) membranes, blocking the filter with milk, and binding radiolabeled IFN-αA to the membrane Filter, with detection by either autoradiography or scintillation counting. This assay procedure has been applied for the identification of IFN-α receptors in crude and affinity-purified fractions. The partially purified IFN-α receptors have been further characterized by SDS-polyacrylamide gel electrophoresis(PAGE). The separated IFN-α receptor protein on the SDS-PAGE gel has been electrophoretically transferred to Immobilon membrane and visualized by ligand blotting. This provides an estimate of 95–110 kD for the apparent molecular weight and a tool for further studies of the receptor protein.
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