Literature DB >> 3090197

Immunoreactivity of a synthetic pentadecapeptide corresponding to the N-terminal region of the scrapie prion protein.

M Shinagawa, E Munekata, S Doi, K Takahashi, H Goto, G Sato.   

Abstract

A pentadecapeptide with an amino acid sequence corresponding to the amino-terminal region of the scrapie prion protein was synthesized. Immunization of a rabbit with the peptide conjugated with ovalbumin induced specific antibodies. The antibodies reacted with all three of the major polypeptides in a proteinase K-treated fraction obtained from brains of mice infected with the Obihiro strain of scrapie agent. Some peptides in the proteinase-untreated fraction also shared antigenicity with the three major polypeptides. Specific polypeptides were also detected by the antiserum in a fraction prepared from spleens, but only two of the three major polypeptides were found and the amounts of the polypeptides were less than in brain.

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Year:  1986        PMID: 3090197     DOI: 10.1099/0022-1317-67-8-1745

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  13 in total

1.  Upregulation of the genes encoding lysosomal hydrolases, a perforin-like protein, and peroxidases in the brains of mice affected with an experimental prion disease.

Authors:  J Kopacek; S Sakaguchi; K Shigematsu; N Nishida; R Atarashi; R Nakaoke; R Moriuchi; M Niwa; S Katamine
Journal:  J Virol       Date:  2000-01       Impact factor: 5.103

Review 2.  Prion liposomes.

Authors:  R Gabizon; S B Prusiner
Journal:  Biochem J       Date:  1990-02-15       Impact factor: 3.857

3.  Immunohistochemical detection of prion protein in lymphoid tissues of sheep with natural scrapie.

Authors:  L J van Keulen; B E Schreuder; R H Meloen; G Mooij-Harkes; M E Vromans; J P Langeveld
Journal:  J Clin Microbiol       Date:  1996-05       Impact factor: 5.948

4.  Improvement of PrPSc-detection in mouse spleen early at the preclinical stage of scrapie with collagenase-completed tissue homogenization and Sarkosyl-NaCl extraction of PrPSc.

Authors:  K U Grathwohl; M Horiuchi; N Ishiguro; M Shinagawa
Journal:  Arch Virol       Date:  1996       Impact factor: 2.574

5.  Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.

Authors:  T Kitamoto; T Muramoto; S Mohri; K Doh-Ura; J Tateishi
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

6.  Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

Authors:  L Monari; S G Chen; P Brown; P Parchi; R B Petersen; J Mikol; F Gray; P Cortelli; P Montagna; B Ghetti
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-29       Impact factor: 11.205

Review 7.  Inhibition of scrapie-associated PrP accumulation. Probing the role of glycosaminoglycans in amyloidogenesis.

Authors:  S A Priola; B Caughey
Journal:  Mol Neurobiol       Date:  1994 Apr-Jun       Impact factor: 5.590

Review 8.  Impaired motor coordination in mice lacking prion protein.

Authors:  S Katamine; N Nishida; T Sugimoto; T Noda; S Sakaguchi; K Shigematsu; Y Kataoka; A Nakatani; S Hasegawa; R Moriuchi; T Miyamoto
Journal:  Cell Mol Neurobiol       Date:  1998-12       Impact factor: 5.046

9.  The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.

Authors:  T Muramoto; T Kitamoto; J Tateishi; I Goto
Journal:  Am J Pathol       Date:  1992-06       Impact factor: 4.307

10.  Preparation and characterization of antibodies against mouse prion protein (PrP) peptides.

Authors:  T Yokoyama; K Kimura; Y Tagawa; N Yuasa
Journal:  Clin Diagn Lab Immunol       Date:  1995-03
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