Radioactive labeling of recombinant antibody fragments by phosphorylation using human casein kinase II and [γ-32P]-ATP
- 1 April 1996
- journal article
- research article
- Published by Springer Nature in Nature Biotechnology
- Vol. 14 (4) , 485-490
- https://doi.org/10.1038/nbt0496-485
Abstract
A wide range of antibody fragments can be expressed in bacteria and detected immunochemically via peptide tags. Using specially designed tags, we have developed a strategy for radiolabeling antibody fragments secreted from bacteria. Tagged antibody fragments were secreted either into the bacterial periplasm or the culture medium. The tag was not subject to proteolysis either in the broth or in human plasma. After affinity purification the antibody fragments were phosphorylated with [γ-32P]ATP and casein kinase II. The labeled fragments were used in a gel band-shift assay to measure antigen binding affinities. In contrast to non site-specific methods such as radioiodination, antibodies labeled with casein kinase II retain full immunoreactivity. Radioactively phosphorylated antibody fragments may have many other applications, including radioimmunoassays and radioimmunotherapy.Keywords
This publication has 32 references indexed in Scilit:
- High-affinity Antigen Binding by Chelating Recombinant Antibodies (CRAbs)Journal of Molecular Biology, 1995
- In Vitro Assembly of Repertoires of Antibody Chains on the Surface of Phage by RenaturationJournal of Molecular Biology, 1994
- Phage libraries for generation of clinically useful antibodiesThe Lancet, 1994
- Interaction of barnase with its polypeptide inhibitor barstar studied by protein engineeringBiochemistry, 1993
- Blotting and band-shifting: techniques for studying protein-protein interactionsTrends in Biochemical Sciences, 1992
- Making antibody fragments using phage display librariesNature, 1991
- Review Radiolabelled monoclonal antibodies in oncology III. RadioimmunotherapyNuclear Medicine Communications, 1991
- Phage antibodies: filamentous phage displaying antibody variable domainsNature, 1990
- Binding activities of a repertoire of single immunoglobulin variable domains secreted from Escherichia coliNature, 1989
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970