Related references
Note: Only part of the references are listed.Formation of native prions from minimal components in vitro
Nathan R. Deleault et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Converting the prion protein: What makes the protein infectious
Ilia V. Baskakov et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2007)
Site-specific conformational studies of prion protein (PrP) amyloid fibrils revealed two cooperative folding domains within amyloid structure
Ying Sun et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Nonpolar substitution at the C-terminus of the prion protein, a mimic of the glycosylphosphatidylinositol anchor, partially impairs amyloid fibril formation
Leonid Breydo et al.
BIOCHEMISTRY (2007)
Probing the conformation of the prion protein within a single amyloid fibril using a novel immunoconformational assay
Vera Novitskaya et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Dichotomous versus palm-type mechanisms of lateral assembly of amyloid fibrils
Natallia Makarava et al.
PROTEIN SCIENCE (2006)
Polymorphism and ultrastructural organization of prion protein amyloid fibrils: An insight from high resolution atomic force microscopy
M Anderson et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation
L Breydo et al.
BIOCHEMISTRY (2005)
Molecular-level secondary structure, polymorphism, and dynamics of full-length α-synuclein fibrils studied by solid-state NMR
H Heise et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Search for a prion-specific nucleic acid
JG Safar et al.
JOURNAL OF VIROLOGY (2005)
Ethanol-perturbed amyloidogenic self-assembly of insulin: Looking for origins of amyloid strains
W Dzwolak et al.
BIOCHEMISTRY (2005)
Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob disease
OV Bocharova et al.
PROTEIN SCIENCE (2005)
Fibril conformation as the basis of species- and strain-dependent seeding specificity of mammalian prion amyloids
EM Jones et al.
CELL (2005)
In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrPSc
OV Bocharova et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Strain-specified characteristics of mouse synthetic prions
G Legname et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Self-propagating, molecular-level polymorphism in Alzheimer's β-amyloid fibrils
AT Petkova et al.
SCIENCE (2005)
Molecular basis of barriers for interspecies transmissibility of mammalian prions
DL Vanik et al.
MOLECULAR CELL (2004)
The peculiar nature of unfolding of the human prion protein
IV Baskakov et al.
PROTEIN SCIENCE (2004)
Discriminating scrapie and bovine spongiform encephalopathy isolates by infrared spectroscopy of pathological prion protein
A Tomzig et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
RNA molecules stimulate prion protein conversion
NR Deleault et al.
NATURE (2003)
Pathway complexity of prion protein assembly into amyloid
IV Baskakov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
A change in the conformation of prions accompanies the emergence of a new prion strain
D Peretz et al.
NEURON (2002)
DNA converts cellular prion protein into the β-sheet conformation and inhibits prion peptide aggregation
Y Cordeiro et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Strains of [PSI+] are distinguished by their efficiencies of prion-mediated conformational conversion
SM Uptain et al.
EMBO JOURNAL (2001)
Strain-specified relative conformational stability of the scrapie prion protein
D Peretz et al.
PROTEIN SCIENCE (2001)
Share Paper
