Inhibition of cryoprecipitation of murine IgG3 anti‐dinitrophenyl (DNP) monoclonal antibodies by anionic DNP‐amino acid conjugates
- 1 February 1989
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 19 (2) , 273-278
- https://doi.org/10.1002/eji.1830190209
Abstract
Previously we have demonstrated that eight out of nine IgG3 monoclonal antibodies (mAb) obtained from autoimmune MRL‐lpr/lpr mice were able to self‐associate and to precipitate in the cold (Gyotoku et al., J. Immunol. 1987. 138: 3785). To determine whether the cryoprecipitation of IgG3 mAb is enhanced or inhibited in the presence of specific ligand, we have established eight IgG3 mAb reactive with 2,4‐dinitrophenol (DNP) hapten: four mAb were obtained from fusion of spleen cells of C57BL/6 mice immunized with 2,4, 6‐trinitrophenylated keyhole limpet hemocyanin, three from 129/Sv and one from BALB/c immunized with DNP‐lipopolysaccharide. Five of them induced cryoglobulins composed exclusively of the IgG3 mAb. The binding of negatively charged monomeric DNP‐amino acid conjugates completely inhibited the cryoprecipitation of all the five cryoprecipitating anti‐DNP IgG3 mAb, while the incubation with positively charged or neutral DNP‐amino acid conjugates had variable effects: increase, inhibition or no change of the cryoprecipitation. In addition, positively charged DNP‐amino acid conjugates were able to induce the cryoprecipitation of one of the non‐cryoprecipitating anti‐DNP IgG3 mAb. Our data showed that (a) IgG3 mAb derived from non‐autoimmune strains of mice, similar to IgG3 mAb derived from an autoimmune MRL‐lpr/lpr strain, possessed the unique property to self‐associate and were able to form cryoglobulins in most cases; (b) although the Fc‐Fc interactions of IgG3 mAb play a decisive role in IgG3 cold solubility, IgG3 cryoprecipitation was markedly influenced after interacting with their specific ligand, depending on the charge of the hapten‐amino acid conjugate. This suggested that even minor interferences with the electrostatic equilibrium of the IgG3 by the binding of charged hapten molecules induced dramatic changes in the solubility of the IgG3 mAb at low temperature.This publication has 29 references indexed in Scilit:
- Experimental model of murine cryoglobulinemia induced by monoclonal antibodies and modulation by anti-idiotypic AntibodiesSpringer Seminars in Immunopathology, 1988
- Hydrophobicity of Amino Acid Residues in Globular ProteinsScience, 1985
- Partial amino acid sequence of the V region of A κ-type Bence Jones cryoproteinImmunochemistry, 1978
- Molecular basis for the temperature-dependent insolubility of cryoglobulins—IV: Structural studies of the IgM monoclonal cryoglobulin McEImmunochemistry, 1978
- Amino acid properties and side-chain orientation in proteins: A cross correlation approachJournal of Theoretical Biology, 1975
- A NEW MOUSE IMMUNOGLOBULIN: IGG3The Journal of Experimental Medicine, 1971
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- Aggregation of γG3 proteins: relevance to the hyperviscosity syndromeJournal of Clinical Investigation, 1970
- Decreased tyrosine/tryptophan ratio in a 6.6S cryoglobulin, as determined by a spectrophotometric techniqueBiochemical and Biophysical Research Communications, 1968
- Human monoclonal γG-cryoglobulins with anti—γ-globulin activityJournal of Clinical Investigation, 1968