IMMUNOHISTOCHEMICAL STUDY OF KURU PLAQUES USING ANTIBODIES AGAINST SYNTHETIC PRION PROTEIN-PEPTIDES

被引:28
作者
HASHIMOTO, K [1 ]
MANNEN, T [1 ]
NUKINA, N [1 ]
机构
[1] UNIV TOKYO,INST BRAIN RES,DEPT NEUROL,7-3-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
关键词
AMYLOID; CREUTZFELDT-JAKOB DISEASE; GERSTMANN-STRAUSSLER SYNDROME; KURU PLAQUE; PRION PROTEIN;
D O I
10.1007/BF00299410
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Prion protein (PrP) is a protein closely associated with the transmission of scrapie and Creutzfeldt-Jakob disease (CJD). Kuru plaques are composed of this protein. PrP33-35 is converted to protease-resistant PrP27-30 by proteinase K digestion. It has not yet been determined which of these PrPs is present in kuru plaques in vivo. Accordingly we synthesized two peptides (peptide-N and peptide-M) that, respectively, corresponded to the protease-sensitive and protease-resistant portions of PrP33-35, based on the amino acid sequence deduced from human PrP cDNA. These two synthetic peptides were used to immunize rabbits and produce antisera (anti-N and anti-M). Both antisera stained kuru plaques in a patient with Gerstmann-Straussler syndrome and one with CJD. Peptide-N has an amino acid sequence which does not exist in PrP27-30. Staining of kuru plaques by the antiserum against peptide-N indicated that the entire molecule, including the N-terminal portion of PrP33-35, was deposited in the kuru plaques.
引用
收藏
页码:613 / 617
页数:5
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