Literature DB >> 3300520

Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes.

J M Bockman, S B Prusiner, J Tateishi, D T Kingsbury.   

Abstract

Creutzfeldt-Jakob disease (CJD) is a rare dementia that is generally found in older people and is caused by unusual infectious pathogens or prions. Using rabbit antisera raised against hamster scrapie prion proteins (HaPrPSc), we identified by immunoblotting human CJD prion proteins (HuPrPCJD) in the brains of 14 patients dying of CJD. Extracts from 6 of the patients were transmitted to mice after prolonged incubation. The rabbit antisera raised against HaPrPSc also reacted with the mouse CJD prion proteins (MoPrPCJD) found in the brains of these experimentally infected mice. When mice were immunized with HuPrPCJD, they produced antibodies that reacted with HuPrPCJD but not with MoPrPCJD. Mice immunized with MoPrPCJD produced antibodies to neither murine nor human prion proteins. Our results provide evidence for host species-specific epitopes on prion proteins. The existence of such epitopes is consistent with the apparent lack of an immune response during prion infections and the finding that prion protein molecules are encoded by host genes.

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Year:  1987        PMID: 3300520     DOI: 10.1002/ana.410210611

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  14 in total

Review 1.  Prion liposomes.

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

2.  Immunological analysis of host and agent effects on Creutzfeldt-Jakob disease and scrapie prion proteins.

Authors:  J M Bockman; D T Kingsbury
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

3.  Temporal evolution of electroencephalographic abnormalities in Creutzfeldt-Jakob disease.

Authors:  G K Schlenska; G F Walter
Journal:  J Neurol       Date:  1989-12       Impact factor: 4.849

4.  Immunoaffinity purification and neutralization of scrapie prion infectivity.

Authors:  R Gabizon; M P McKinley; D Groth; S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

5.  Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Authors:  R A Bessen; R F Marsh
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

6.  IP10, KC and M-CSF Are Remarkably Increased in the Brains from the Various Strains of Experimental Mice Infected with Different Scrapie Agents.

Authors:  Jia Chen; Cao Chen; Chao Hu; Lian Liu; Ying Xia; Lin Wang; Wei Yang; Hai-Yan Wu; Wei Zhou; Kang Xiao; Qi Shi; Yuezhang Wu; Zhi-Bao Chen; Xiao-Ping Dong
Journal:  Virol Sin       Date:  2020-04-20       Impact factor: 4.327

7.  Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

Authors:  R Gabizon; H Rosenmann; Z Meiner; I Kahana; E Kahana; Y Shugart; J Ott; S B Prusiner
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

8.  Chimeric prion protein expression in cultured cells and transgenic mice.

Authors:  M R Scott; R Köhler; D Foster; S B Prusiner
Journal:  Protein Sci       Date:  1992-08       Impact factor: 6.725

Review 9.  Neurodegeneration in humans caused by prions.

Authors:  S B Prusiner
Journal:  West J Med       Date:  1994-09

10.  Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins.

Authors:  D A Butler; M R Scott; J M Bockman; D R Borchelt; A Taraboulos; K K Hsiao; D T Kingsbury; S B Prusiner
Journal:  J Virol       Date:  1988-05       Impact factor: 5.103

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