A chicken monoclonal antibody with specificity for the N-terminal of human prion protein

被引:43
|
作者
Matsuda, H
Mitsuda, H
Nakamura, N
Furusawa, S
Mohri, S
Kitamoto, T
机构
[1] Hiroshima Univ, Fac Appl Biol Sci, Dept Immunobiol, Higashihiroshima, Hiroshima 7398528, Japan
[2] Kyushu Univ, Fac Med, Biomed Res Ctr, Fukuoka 8128582, Japan
[3] Tohoku Univ, Sch Med, Dept Neurol Sci, Aoba Ku, Sendai, Miyagi 9808575, Japan
来源
关键词
chicken monoclonal antibody; prion protein; Creutzfeldt-Jakob disease; Gerstmann-Straussler syndrome;
D O I
10.1016/S0928-8244(98)00135-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chickens were immunized with human prion protein (PrP) peptide H25 (amino acid residues 25-49) coupled to keyhole limpet hemocyanin. From a fusion experiment using the chicken fusion partner cell line MuH1 and immune spleen cells, one mAb, HUC2-13, was generated which reacted with the peptide. HUC2-13 was specific for a pentapeptide (RPKPG) of the N-terminal of the peptide H25. Tn Western blotting analysis, the mAb reacted with PrP materials from a human Creutzfeldt-Jakob disease (CJD) case and the membrane fraction from normal murine brain,but not with the same materials pretreated with proteinase K. When compared with the HUC2-13 and the conventional mouse mAb 3F4, the background stainings using the HUC2-13 were minimal. In immunohistochemistry, the HUC2-13 stained positively with kuru plaques in brain sections from patients with Gerstmann-Straussler syndrome (GSS), and also reacted with synaptic structures of the CJD patients. However, any immunolabelings using the HUC2-13 were not observed in the section from a patient with amyotrophic lateral sclerosis (ALS) as CJD-negative control. These results indicate that the mAb HUC2-13 is a suitable tool for immunological and diagnostic analyses of prion disease in humans and other mammals. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 194
页数:6
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