Publication | Closed Access
Analysis of autoantibody binding to 52‐kd paraneoplastic cerebellar degeneration–associated antigen expressed in recombinant proteins
51
Citations
22
References
1993
Year
Laboratory ImmunologyImmunologyImmunoeditingPathologyAntigen ProcessingImmunotherapeuticsAntigen Cdr62Tumor BiologyParaneoplastic CerebellarNeuroimmunologyHistopathologyImmune SurveillanceCell BiologyCommon EpitopeNeurodegenerative DiseasesRecombinant ProteinsTumoral PathologyMajor EpitopeDegenerative DiseaseMolecular NeurobiologyMedicineCell DevelopmentImmunological Biomarkers
Abstract A 52‐kd neural antigen was reported to be recognized by anti‐Purkinje cell antibodies in serum of a patient with paraneoplastic cerebellar degeneration associated with uterine carcinoma. In this study, we demonstrate that this neural antigen is recognized by antibodies known as anti‐Purkinje cell antibody type I (PCAb Type I) and anti‐YO. The latter's antigen is reported to be specific for the 62‐ to 64‐kd antigen CDR62. Assuming that the 52‐kd and 62‐ to 64‐kd antigens share a common epitope(s) recognized by all of these antibodies, we examined the antigenic region on the 52‐kd protein by immunoblots with deletion fragment proteins of the recombinant 52‐kd protein. A major epitope was localized in the region of amino acid residues 94 to 133 of the 52‐kd protein, which is the site of a leucine zipper motif. The potential pathogenicity of PCAb Type I is discussed.
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