(Q54014606)

23 May 2018

title

Inhibition of interactions and interconversions of prion protein isoforms by peptide fragments from the C-terminal folded domain. (English)

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23 May 2018

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Horiuchi M

1

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23 May 2018

Baron GS

series ordinal

2

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23 May 2018

Xiong LW

series ordinal

3

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23 May 2018

Caughey B

series ordinal

4

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23 May 2018

language of work or name

English

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publication date

1 February 2001

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23 May 2018

Journal of Biological Chemistry

published in

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23 May 2018

volume

276

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23 May 2018

issue

18

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23 May 2018

page(s)

15489-15497

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23 May 2018

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

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Normal host prion protein necessary for scrapie-induced neurotoxicity.

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Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

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Chimeric prion protein expression in cultured cells and transgenic mice

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Chaperone-supervised conversion of prion protein to its protease-resistant form

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Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

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

21 January 2018

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Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform

21 January 2018

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Molecular properties of complexes formed between the prion protein and synthetic peptides.

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Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

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Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

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Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

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COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform

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Evidence that the Transmission of One Source of Scrapie Agent to Hamsters Involves Separation of Agent Strains from a Mixture

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Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

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Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

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Prion (PrPSc)-specific epitope defined by a monoclonal antibody

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

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Recombinant scrapie-like prion protein of 106 amino acids is soluble

21 January 2018

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Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

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An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

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PrP genotype contributes to determining survival times of sheep with natural scrapie.

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Inhibition of protease-resistant prion protein formation by porphyrins and phthalocyanines

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Mimicking dominant negative inhibition of prion replication through structure-based drug design

21 January 2018

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Porphyrin and phthalocyanine antiscrapie compounds.

21 January 2018

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Elimination of prions by branched polyamines and implications for therapeutics

21 January 2018

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Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation

21 January 2018

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Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

21 January 2018

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Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides

21 January 2018

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Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state

21 January 2018

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Methods for studying prion protein (PrP) metabolism and the formation of protease-resistant PrP in cell culture and cell-free systems. An update

21 January 2018

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Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides

21 January 2018

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Determination of protein secondary structure in solution by vacuum ultraviolet circular dichroism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M100288200

1 reference

23 May 2018

1 reference

23 May 2018