Journal of Clinical Microbiology · 1992 · 173 citations · 17 references
Life SciencesImmunologyInfectious DiseasesMolecular VirologyMonoclonal AntibodiesVirologyAntibody CharacterizationDiagnostic ImmunologyRecombinant AntibodiesViral DiagnosticsViral InfectionsAntibodiesDiagnostic Enzyme AssaysEnzyme ImmunoassaysImmunoassaysPolyacrylamide Gel ElectrophoresisRecombinant Protein AntigensSodium Dodecyl Sulfate-polyacrylamide Gel ElectrophoresisViral Antigen Detection
A recombinant baculovirus that expresses the nucleoprotein gene of measles virus (Edmonston vaccine strain) under the transcriptional control of the polyhedrin promoter was generated. The expressed protein (B-MVN) comigrated with the authentic viral nucleoprotein as observed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and it was phosphorylated. The B-MVN protein proved to be reactive with monoclonal antibodies in radioimmunoprecipitations, and it was immunogenic, eliciting in mice antisera that recognized the native nucleoprotein. In addition, the B-MVN protein was evaluated as a replacement source of antigen for whole virus in enzyme immunoassays (EIAs) for detection of measles virus-specific immunoglobulin M (IgM) and IgG antibodies. A capture IgM EIA with the B-MVN protein as antigen detected specific IgM antibodies in 18 (72%) acute- and all convalescent-phase specimens from 25 clinical measles cases and exceeded 99% specificity with 120 control specimens. An indirect IgG EIA with the B-MVN protein detected specific IgG antibodies in 129 of 131 (98%) serum specimens with antibodies to measles virus, and results obtained from testing 268 additional serum specimens were better correlated with measles virus-neutralizing antibodies than those obtained with a commercial EIA.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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