The Journal of Immunology · 1985 · 30 citations · 0 references
Life SciencesImmunologyMolecular BiologyAutoimmunityMolecular ImmunologyMonoclonal AntibodiesAntibody CharacterizationAntibody PurificationAntibody-antigen RecognitionAntigen RecognitionAutoantibodiesEpitope MappingAnti-double-stranded Dna AntibodiesAntibodiesAntibody Binding SpecificityAntibody Epitope MappingAntibody Specificity AnalysisAntigen Specificity DeterminationAntigen-antibody InteractionsAntigen-antibody Recognition
Six anti-DNA hybridoma autoantibodies were prepared by fusing spleen cells from unimmunized MRL/MpJ/lpr/lpr female mice with BALB/c myeloma cells. The monoclonal antibodies were analyzed by solid-phase ELISA for antigen-binding specificities. Three antibodies (62A2, 85A5, and 43B2) bound ssDNA, TNP-KLH, and recognized an epitope(s) present on insolubilized proteins such as BSA, KLH, ferritin, and insulin. The antibodies bound, with a marked preference, TNP-KLH, either soluble or insoluble. The other three antibodies (35A1, 32C5, and 39D2) bound only ssDNA. However, this binding was inhibited by free flavinic acid. None of the six antibodies bound either cardiolipin or proteoglycans, indicating that they do not recognize the repeating negatively charge units common to cardiolipin, proteoglycans, and DNA. All six monoclonal antibodies were purified by affinity chromatography with TNP-Sepharose. Moreover, both anti-DNA and anti-TNP antibodies from sera of nonautoimmune and autoimmune mice were purified easily on TNP-Sepharose.