TY - JOUR
T1 - Detection and Analysis of Interferon-α Receptors on Plasma Membranes and in Detergent Extracts
AU - Puvanakrishnan, Rengarajulu
AU - Langer, Jerome A.
PY - 1990/6
Y1 - 1990/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0025280792&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025280792&partnerID=8YFLogxK
U2 - 10.1089/jir.1990.10.299
DO - 10.1089/jir.1990.10.299
M3 - Article
C2 - 2143524
AN - SCOPUS:0025280792
SN - 0197-8357
VL - 10
SP - 299
EP - 307
JO - Journal of Interferon Research
JF - Journal of Interferon Research
IS - 3
ER -