A prion protein epitope selective for the pathologically misfolded conformation (Q34201802)

31 July 2017

title

A prion protein epitope selective for the pathologically misfolded conformation (English)

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31 July 2017

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James Ironside

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31 July 2017

Harry C Ledebur

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Avi Chakrabartty

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Mark Head

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Neil R Cashman

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31 July 2017

Katherine I. O'Rourke

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Katherine O'Rourke

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31 July 2017

Robert Will

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31 July 2017

author name string

Eustache Paramithiotis

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31 July 2017

Marc Pinard

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31 July 2017

Trebor Lawton

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31 July 2017

Sylvie LaBoissiere

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31 July 2017

Valerie L Leathers

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31 July 2017

Wen-Quan Zou

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31 July 2017

Lisa A Estey

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31 July 2017

Julie Lamontagne

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31 July 2017

Marty T Lehto

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31 July 2017

Leslie H Kondejewski

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31 July 2017

Gregory P Francoeur

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31 July 2017

Maria Papadopoulos

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31 July 2017

Ashkan Haghighat

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31 July 2017

Stephen J Spatz

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31 July 2017

Quentin Tonelli

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31 July 2017

language of work or name

English

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publication date

1 July 2003

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31 July 2017

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

893-899

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31 July 2017

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

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Semipreparative chromatographic method to purify the normal cellular isoform of the prion protein in nondenatured form.

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Binding of disease-associated prion protein to plasminogen.

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pH-dependent Stability and Conformation of the Recombinant Human Prion Protein PrP(90–231)

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A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH.

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Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

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Oxygen and acrylamide quenching of protein phosphorescence: correlation with protein dynamics

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NMR structure of the mouse prion protein domain PrP(121-231)

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Solution structure of Syrian hamster prion protein rPrP(90-231).

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NMR solution structure of the human prion protein

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Cloning and characterization of cDNAs encoding four different canine immunoglobulin gamma chains

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Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form

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Scrapie-Infected Spleens: Analysis of Infectivity, Scrapie-Associated Fibrils, and Protease-Resistant Proteins

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Detection of proteinase K-resistant prion protein and infectivity in mouse spleen by 2 weeks after scrapie agent inoculation

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Kinetics of prion protein accumulation in the CNS of mice with experimental scrapie

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CNA42 monoclonal antibody identifies FDC as PrPsc accumulating cells in the spleen of scrapie affected sheep

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Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

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The immunobiology of TSE diseases.

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Eight prion strains have PrP(Sc) molecules with different conformations

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Species-barrier-independent prion replication in apparently resistant species

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Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers

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Prion research: the next frontiers

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Complement facilitates early prion pathogenesis

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Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie.

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A crucial role for B cells in neuroinvasive scrapie.

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Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody

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Antibodies inhibit prion propagation and clear cell cultures of prion infectivity

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Signal transduction through prion protein

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Cellular isoform of the scrapie agent protein participates in lymphocyte activation

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Nearly ubiquitous tissue distribution of the scrapie agent precursor protein

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Monoclonal antibodies inhibit prion replication and delay the development of prion disease

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Structural studies of the scrapie prion protein by electron crystallography

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A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform 1 1Edited by M. Yaniv

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Scrapie amyloid (prion) protein has the conformational characteristics of an aggregated molten globule folding intermediate

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7 January 2021

Identifiers

DOI

10.1038/NM883

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31 July 2017

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