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Fibril Conformation as the Basis of Species- and Strain-Dependent Seeding Specificity of Mammalian Prion Amyloids

Cell, 2005-04, Vol.121 (1), p.63-72

2005

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The Effect of Disease-associated Mutations on the Folding Pathway of Human Prion Protein

The Journal of biological chemistry, 2004-04, Vol.279 (17), p.18008-18014

2004

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On the Mechanism of α-Helix to β-Sheet Transition in the Recombinant Prion Protein

Biochemistry (Easton), 2001-06, Vol.40 (23), p.6982-6987

2001

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Molecular Basis of Barriers for Interspecies Transmissibility of Mammalian Prions

Molecular cell, 2004-04, Vol.14 (1), p.139-145

2004

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Crystal structure of the human prion protein reveals a mechanism for oligomerization

Nature structural & molecular biology, 2001-09, Vol.8 (9), p.770-774

2001

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Determination of protein secondary structure by Fourier transform infrared spectroscopy: A critical assessment

Biochemistry (Easton), 1993-01, Vol.32 (2), p.389-394

1993

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Nucleation-Dependent Conformational Conversion of the Y145Stop Variant of Human Prion Protein: Structural Clues for Prion Propagation

Proceedings of the National Academy of Sciences - PNAS, 2003-10, Vol.100 (21), p.12069-12074

2003

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Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

Cellular and molecular life sciences : CMLS, 2008-02, Vol.65 (4), p.631-643, Article 631

2008

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Polymorphism at Residue 129 Modulates the Conformational Conversion of the D178N Variant of Human Prion Protein 90−231

Biochemistry (Easton), 2005-12, Vol.44 (48), p.15880-15888

2005

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Membrane Environment Alters the Conformational Structure of the Recombinant Human Prion Protein

The Journal of biological chemistry, 1999-12, Vol.274 (52), p.36859-36865

1999

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Aggregation and Fibrillization of the Recombinant Human Prion Protein huPrP90−231

Biochemistry (Easton), 2000-01, Vol.39 (2), p.424-431

2000

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Kinetic Intermediate in the Folding of Human Prion Protein

The Journal of biological chemistry, 2002-11, Vol.277 (47), p.44589-44592

2002

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The Prion Protein Has RNA Binding and Chaperoning Properties Characteristic of Nucleocapsid Protein NCp7 of HIV-1

The Journal of biological chemistry, 2001-06, Vol.276 (22), p.19301-19309

2001

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Conformational diversity in prion protein variants influences intermolecular β-sheet formation

The EMBO journal, 2010-01, Vol.29 (1), p.251-262

2010

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pH-dependent structural transitions of Alzheimer amyloid peptides

Biophysical journal, 1991-11, Vol.60 (5), p.1190-1201

1991

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Atypical Effect of Salts on the Thermodynamic Stability of Human Prion Protein

The Journal of biological chemistry, 2003-06, Vol.278 (25), p.22187-22192

2003

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

The Journal of biological chemistry, 1997-10, Vol.272 (44), p.27517-27520

1997

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The Role of Disulfide Bridge in the Folding and Stability of the Recombinant Human Prion Protein

The Journal of biological chemistry, 2001-01, Vol.276 (4), p.2427-2431

2001

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Acceleration of Amyloid Fibril Formation by Specific Binding of Aβ-(1–40) Peptide to Ganglioside-containing Membrane Vesicles

The Journal of biological chemistry, 1997-09, Vol.272 (37), p.22987-22990

1997

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Disease-associated F198S Mutation Increases the Propensity of the Recombinant Prion Protein for Conformational Conversion to Scrapie-like Form

The Journal of biological chemistry, 2002-12, Vol.277 (50), p.49065-49070

2002

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Familial Mutations and the Thermodynamic Stability of the Recombinant Human Prion Protein

The Journal of biological chemistry, 1998-11, Vol.273 (47), p.31048-31052

1998

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Temperature-induced exposure of hydrophobic surfaces and its effect on the chaperone activity of α-crystallin

FEBS letters, 1995-08, Vol.369 (2), p.321-325

1995

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Fibril formation by primate, rodent, and Dutch-hemorrhagic analogs of Alzheimer amyloid .beta.-protein

Biochemistry (Easton), 1992-11, Vol.31 (44), p.10716-10723

1992

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Membrane binding induces destabilization of cytochrome c structure

Biochemistry (Easton), 1991-07, Vol.30 (29), p.7219-7224

1991

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Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

The Journal of biological chemistry, 2000-10, Vol.275 (43), p.33650-33654

2000

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Fibril Conformation as the Basis of Species- and Strain-Dependent Seeding Specificity of Mammalian Prion Amyloids

The Effect of Disease-associated Mutations on the Folding Pathway of Human Prion Protein

On the Mechanism of α-Helix to β-Sheet Transition in the Recombinant Prion Protein

Molecular Basis of Barriers for Interspecies Transmissibility of Mammalian Prions

Crystal structure of the human prion protein reveals a mechanism for oligomerization

Determination of protein secondary structure by Fourier transform infrared spectroscopy: A critical assessment

Nucleation-Dependent Conformational Conversion of the Y145Stop Variant of Human Prion Protein: Structural Clues for Prion Propagation

Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions

Polymorphism at Residue 129 Modulates the Conformational Conversion of the D178N Variant of Human Prion Protein 90−231

Membrane Environment Alters the Conformational Structure of the Recombinant Human Prion Protein

Aggregation and Fibrillization of the Recombinant Human Prion Protein huPrP90−231

Kinetic Intermediate in the Folding of Human Prion Protein

The Prion Protein Has RNA Binding and Chaperoning Properties Characteristic of Nucleocapsid Protein NCp7 of HIV-1

Conformational diversity in prion protein variants influences intermolecular β-sheet formation

pH-dependent structural transitions of Alzheimer amyloid peptides

Atypical Effect of Salts on the Thermodynamic Stability of Human Prion Protein

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

The Role of Disulfide Bridge in the Folding and Stability of the Recombinant Human Prion Protein

Acceleration of Amyloid Fibril Formation by Specific Binding of Aβ-(1–40) Peptide to Ganglioside-containing Membrane Vesicles

Disease-associated F198S Mutation Increases the Propensity of the Recombinant Prion Protein for Conformational Conversion to Scrapie-like Form

Familial Mutations and the Thermodynamic Stability of the Recombinant Human Prion Protein

Temperature-induced exposure of hydrophobic surfaces and its effect on the chaperone activity of α-crystallin

Fibril formation by primate, rodent, and Dutch-hemorrhagic analogs of Alzheimer amyloid .beta.-protein

Membrane binding induces destabilization of cytochrome c structure

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

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