The utility of photo-affinity labels as ‘mapping’ reagents. A study of sub-populations of a specific rabbit antibody by using structurally related photo-affinity reagents
- 1 July 1974
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 141 (1) , 51-56
- https://doi.org/10.1042/bj1410051
Abstract
A specific rabbit antibody against the 4-azido-2-nitrophenyl determinant was photo-labelled by the homologous hapten ε-(4-azido-2-nitrophenyl)-l-lysine, and by the close structural isomer ε-(5-azido-2-nitrophenyl)-l-lysine. The extents of covalent labelling of the antibody-binding site were assessed by using radioactive haptens and exhaustive displacement dialysis, which leaves the unlabelled sites empty but largely intact. A single photolysis of hapten–antibody complex suffices to label those sites that are capable of being labelled. Although there is considerable overlap among sub-populations of antibody that will bind the two haptens non-covalently, sites that can be covalently labelled by one reagent cannot be labelled by the other.Keywords
This publication has 7 references indexed in Scilit:
- Affinity labelling of the binding site of rabbit antibody. Evidence for the involvement of the hypervariable regions of the heavy chainBiochemical Journal, 1974
- Dynamics of hapten-antibody interaction. Studies on a myeloma protein with anti-2, 4-dinitrophenyl specificityJournal of Molecular Biology, 1972
- The antibody binding site. Labelling of a specific antibody against the photo-precursor of an aryl nitreneBiochemical Journal, 1972
- Affinity Labeling of the Heavy and Light Chains of a Myeloma Protein with Anti-2,4-Dinitrophenyl ActivityProceedings of the National Academy of Sciences, 1970
- Allotype-related sequence variation of the heavy chain of rabbit immunoglobulin GBiochemical Journal, 1968
- THE PARTICIPATION OF A AND B POLYPEPTIDE CHAINS IN THE ACTIVE SITES OF ANTIBODY MOLECULESProceedings of the National Academy of Sciences, 1964
- AMINO ACID COMPOSITIONS OF HUMAN AND RABBIT γ-GLOBULINS AND OF THE FRAGMENTS PRODUCED BY REDUCTIONBiochemical Journal, 1963