Avian Oncornavirus Group-Specific Antigen: Detection and Quantification by Radioimmunoassay

Author:

Fritz Robert B.1,Qualtiere Louis F.1

Affiliation:

1. Department of Microbiology, Division of Basic Health Sciences, Emory University, Atlanta, Georgia 30322

Abstract

A double-antibody competitive-inhibition radioimmunoassay for avian group-specific antigen is described. A viral protein preparation, consisting primarily of gs-1, was labeled with radioiodine. Hamster and rabbit antisera were reacted with the labeled antigen, and the resultant antibody-antigen complexes were precipitated with the appropriate antiglobulin. Standard curves based on the inhibition of binding of labeled antigen to antibody after preincubation with unlabeled antigen were prepared. These showed the lower limit of sensitivity to be 2 to 10 ng of unlabeled protein when labeled antigen of 2,000 to 5,000 counts per min per ng of specific activity was used in the assay. Extracts of avian oncornavirus-infected cells, likewise, were able to inhibit binding of labeled antigen. This technique will be very useful for the quantification of small amounts of oncornavirus group-specific protein.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference18 articles.

1. Ribonucleic acid components of BAI strain A (myeloblastosis) avian tumor virus;Bonar R. A.;Cancer Res.,1967

2. Radioimmune precipitation of group A arboviruses;Dalrymple J. M.;J. Immunol.,1972

3. Immunoprecipitin reaction of influenza virus-antibody complex with anti IgG;Daugharty H.;J. Immunol.,1971

4. Radioiodination of antibodies adsorbed to insoluble antigens;Day E. D.;J. Immunol.,1967

5. Chromatographic separation and antigenic analysis of proteins of the oncornaviruses. I. Avian leukemia-sarcoma viruses;Fleissner E.;J. Virol.,1971

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