A prion protein epitope selective for the pathologically misfolded conformation.
Nat Med
; 9(7): 893-9, 2003 Jul.
Article
en En
| MEDLINE
| ID: mdl-12778138
ABSTRACT
Conformational conversion of proteins in disease is likely to be accompanied by molecular surface exposure of previously sequestered amino-acid side chains. We found that induction of beta-sheet structures in recombinant prion proteins is associated with increased solvent accessibility of tyrosine. Antibodies directed against the prion protein repeat motif, tyrosine-tyrosine-arginine, recognize the pathological isoform of the prion protein but not the normal cellular isoform, as assessed by immunoprecipitation, plate capture immunoassay and flow cytometry. Antibody binding to the pathological epitope is saturable and specific, and can be created in vitro by partial denaturation of normal brain prion protein. Conformation-selective exposure of Tyr-Tyr-Arg provides a probe for the distribution and structure of pathologically misfolded prion protein, and may lead to new diagnostics and therapeutics for prion diseases.
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Banco de datos:
MEDLINE
Asunto principal:
Pliegue de Proteína
/
Proteínas PrPSc
/
Especificidad de Anticuerpos
/
Epítopos
Tipo de estudio:
Diagnostic_studies
Límite:
Animals
/
Humans
Idioma:
En
Año:
2003
Tipo del documento:
Article