(Q44127955)

30 November 2017

DNA-induced partial unfolding of prion protein leads to its polymerisation to amyloid (English)

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30 November 2017

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P K Nandi

1

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30 November 2017

E Leclerc

series ordinal

2

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30 November 2017

J-C Nicole

series ordinal

3

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30 November 2017

M Takahashi

series ordinal

4

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30 November 2017

language of work or name

English

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publication date

1 September 2002

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Journal of Molecular Biology

30 November 2017

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30 November 2017

322

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30 November 2017

1

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30 November 2017

153-161

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https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

30 November 2017

1 reference

Deadly conformations--protein misfolding in prion disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Molecular biology of prion propagation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

The double life of the prion protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Models of amyloid seeding in Alzheimer's disease and scrapie: mechanistic truths and physiological consequences of the time-dependent solubility of amyloid proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

PAN, the proteasome-activating nucleotidase from archaebacteria, is a protein-unfolding molecular chaperone

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Polymerization of murine recombinant prion protein in nucleic acid solution

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Murine recombinant prion protein induces ordered aggregation of linear nucleic acids to condensed globular structures

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Complementary recognition in condensed DNA: accelerated DNA renaturation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

The prion protein has DNA strand transfer properties similar to retroviral nucleocapsid protein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

7 January 2021

Prion Protein Biology

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

The ultrastructural diversity of scrapie-associated fibrils isolated from experimental scrapie and Creutzfeldt-Jakob disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Electronmicroscopic detection of prion-protein-positive fibres in brain from iatrogenic Creutzfeldt-Jakob disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Amyloid fibril formation and seeding by wild-type human lysozyme and its disease-related mutational variants.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Extremely rapid folding of the C-terminal domain of the prion protein without kinetic intermediates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Evidence of molten globule like state(s) of interferon gamma in acidic and sodium perchlorate solutions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Polymerization of human prion peptide HuPrP 106-126 to amyloid in nucleic acid solution.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Coupling of local folding to site-specific binding of proteins to DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Induced folding in RNA-protein recognition: more than a simple molecular handshake

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Evidence for the role of PrP(C) helix 1 in the hydrophilic seeding of prion aggregates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

DNA-induced conformational changes in bacteriophage 434 repressor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Membrane environment alters the conformational structure of the recombinant human prion protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Designing conditions for in vitro formation of amyloid protofilaments and fibrils

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Molecular genetics of transmissible spongiform encephalopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Structure of Bam HI endonuclease bound to DNA: partial folding and unfolding on DNA binding

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

A transmembrane form of the prion protein in neurodegenerative disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Regulation of gene expression by repressor localization: biochemical evidence that membrane and DNA binding by the PutA protein are mutually exclusive

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

7 January 2021

Moonlighting proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

A 'unified theory' of prion propagation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Evolution of amyloid: what normal protein folding may tell us about fibrillogenesis and disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

Energetics of folding and DNA binding of the MAT alpha 2 homeodomain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2836%2802%2900750-7

10.1016/S0022-2836(02)00750-7

7 January 2021

Identifiers

DOI

1 reference

30 November 2017

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