Production and characterization of monoclonal antibody to gentamicin

• Published in: Hybridoma Vol. 3; no. 2; p. 187
• Main Authors: Place, J D, Thompson, S G, Burd, J F, Molinaro, C, Ott, R A, Jensen, F C
• Format: Journal Article
• Language: English
• Published: United States 1984
• Subjects: Animals; Antibodies, Monoclonal - immunology; Antibody Affinity; Electrophoresis, Polyacrylamide Gel; Gentamicins - immunology; Hybridomas - immunology; Mice; Mice, Inbred BALB C; Spleen - cytology
• ISSN: 0272-457X
• DOI: 10.1089/hyb.1984.3.187

Splenocytes from BALB/c mice immunized with a gentamicin-hemocyanin conjugate were fused with X63-Ag8.653 murine myeloma cells to produce hybridomas that secreted monoclonal antibody to gentamicin. Sixteen positive clones were obtained. The monoclonal antibody chosen for a gentamicin immunoassay has been characterized with respect to class, subclass, type of light chain, electrophoretic homogeneity, and binding affinity. Gentamicin monoclonal antibody purified from mouse ascites fluid was analyzed by immunoelectrophoresis, double immunodiffusion, enzyme-linked immunosorbent assay (ELISA), and polyacrylamide gel electrophoresis (PAGE). The results show that the antibody is an IgG2a (kappa). Two bands were detected when the purified antibody was electrophoresed on polyacrylamide gels: a major band and a less mobile minor component (5.6% of the major band). Both were IgG2a (kappa). The major band contained antibody which bound 2.1 moles of the substrate-labeled gentamicin derivative, beta-galactosyl-umbelliferone sisomicin, per mole of IgG, whereas one mole of the minor band bound only 0.095 moles of the substrate-labeled conjugate. The antibody has an affinity constant of 1.22 X 10(10) M-1.