Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Identification of cellular proteins binding to the scrapie prion protein.
B Oesch; D B Teplow; N Stahl; D Serban; L E Hood; S B Prusiner (Profiled Author: Teplow, David B)
Department of Neurology, University of California, San Francisco 94143.
Biochemistry 1990;29(24):5848-55.
The scrapie prion protein (PrPSc) is an abnormal isoform of the cellular protein PrPc. PrPSc is found only in animals with scrapie or other prion diseases. The invariable association of PrPSc with infectivity suggests that PrPSc is a component of the infectious particle. In this study, we report the identification of two proteins from hamster brain of 45 and 110 kDa (denoted PrP ligands Pli 45 and Pli 110) which were able to bind to PrP 27-30, the protease-resistant core of PrPSc on ligand blots. Pli 45 and Pli 110 also bound PrPC. Both Pli's had isoelectric points of approximately 5. The dissociation rate constant of the Pli 45/PrP 27-30 complex was 3 x 10(-6) s-1. Amino acid and protein sequence analyses were performed on purified Pli 45. Both the composition and the sequence were almost identical with those predicted for mouse glial fibrillary acidic protein (GFAP). Furthermore, antibodies to Pli 45 reacted with recombinant GFAP. The identification of proteins which interact with the PrP isoforms in normal and diseased brain may provide new insights into the function of PrPC and into the molecular mechanisms underlying prion diseases.
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Grants
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1.
Rogers, Jack T
RNA Targeted Screens of the Prion 5'UTR
30 September 2008 - 31 August 2010
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 269,917
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2.
LANSBURY, PETER T
PROTEIN CHEMISTRY OF SCRAPIE AND RELATED DISEASES
4 April 1996 - 31 January 2000
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 719,904
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3.
Frangione, Blas
CONFORMATIONAL DISORDERS--AMYLOID AND PRION PROTEINS
1 September 1978 - 31 March 2006
NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES
Total Funding: $ 3,600,812
Related Publications
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1.
1995R A Bessen; D A Kocisko; G J Raymond; S Nandan; P T Lansbury; B Caughey
Non-genetic propagation of strain-specific properties of scrapie prion protein.
Nature 1995;375(6533):698-700. -
2.
1994D A Kocisko; J H Come; S A Priola; B Chesebro; G J Raymond; P T Lansbury; B Caughey
Cell-free formation of protease-resistant prion protein.
Nature 1994;370(6489):471-4. -
3.
1985R I Carp; P A Merz; R J Kascsak; G S Merz; H M Wisniewski
Nature of the scrapie agent: current status of facts and hypotheses.
The Journal of general virology 1985;66 ( Pt 7)():1357-68.
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