Biochemical Journal · 1972 · 153 citations · 16 references
PharmacyBiochemistryImmunologyImmunotechnologyMolecular ImmunologyMonoclonal AntibodiesAntibody CharacterizationAntibody PurificationAntibody StructureAntibody-antigen RecognitionImmunoglobulin FunctionLigand BindingHypervariable Region AnalysisLight Chain Structure
The isolation of specific rabbit antibodies for the haptenic group 4-azido-2-nitrophenyl, is described. These antibodies bind 1.8-2.0mol of hapten [in-(4-azido-2-nitrophenyl)-l-lysine]/mol with an association constant of nearly 10(7)m(-1) at 4 degrees C. On photolysis of the antibody-hapten complex, resulting in the formation of an aryl nitrene at the binding site, hapten was covalently bound to the antibody, and the antibody binding site was blocked. The ratio of labelling of heavy- and light-chains was 2.5:1. Two small peptides were isolated from digests of labelled heavy-chain, indicating that some 13% of the label in the antibody was attached to cysteine-92 and to alanine-93. These residues are adjacent to the major hypervariable region in rabbit heavy-chain (residues 95-105).
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PREPARATION OF PURIFIED ANTI-2,4-DINITROPHENYL ANTIBODIES.
The disulphide bonds of the heavy chain of rabbit immunoglobulin G
Ian O’Donnell, B Frangione, Roy Porter · Biochemical Journal · 1970 · 125 citations · Full text
Allotypically related sequences in the Fd fragment of rabbit immunoglobulin heavy chains
L E Mole, S Jackson, Roy Porter et al. · Biochemical Journal · 1971 · 116 citations · Full text