相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Heparin Binding by Murine Recombinant Prion Protein Leads to Transient Aggregation and Formation of RNA-Resistant Species
Tuane C. R. G. Vieira et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Recombinant prion protein induces a new transmissible prion disease in wild-type animals
Natallia Makarava et al.
ACTA NEUROPATHOLOGICA (2010)
The α-Helical C-Terminal Domain of Full-Length Recombinant PrP Converts to an In-Register Parallel β-Sheet Structure in PrP Fibrils: Evidence from Solid State Nuclear Magnetic Resonance
Robert Tycko et al.
BIOCHEMISTRY (2010)
Conformational diversity in prion protein variants influences intermolecular β-sheet formation
Seungjoo Lee et al.
EMBO JOURNAL (2010)
Tetracysteine-tagged prion protein allows discrimination between the native and converted forms
Jernej Gaspersic et al.
FEBS JOURNAL (2010)
Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors
Jae-Il Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Generating a Prion with Bacterially Expressed Recombinant Prion Protein
Fei Wang et al.
SCIENCE (2010)
Hydrogen/deuterium exchange mass spectrometry identifies two highly protected regions in recombinant full-length prion protein amyloid fibrils
Alexis Nazabal et al.
JOURNAL OF MASS SPECTROMETRY (2009)
The Region Approximately between Amino Acids 81 and 137 of Proteinase K-Resistant PrPSc Is Critical for the Infectivity of the Chandler Prion Strain
Ryo Shindoh et al.
JOURNAL OF VIROLOGY (2009)
Molecular mechanisms for protein-encoded inheritance
Jed J. W. Wiltzius et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2009)
De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis
Christina J. Sigurdson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Design and construction of diverse mammalian prion strains
David W. Colby et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
The same primary structure of the prion protein yields two distinct self-propagating states
Natallia Makarava et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Molecular model of an α-helical prion protein dimer and its monomeric subunits as derived from chemical cross-linking and molecular modeling calculations
T. Kaimann et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Scrapie prion protein structural constraints obtained by limited proteolysis and mass spectrometry
Gustavo Sajnani et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Crystal structure of a stable dimer reveals the molecular basis of serpin polymerization
Masayuki Yamasaki et al.
NATURE (2008)
The POM Monoclonals: A Comprehensive Set of Antibodies to Non-Overlapping Prion Protein Epitopes
Magdalini Polymenidou et al.
PLOS ONE (2008)
Mechanisms of prion protein assembly into amyloid
Jan Stoehr et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Intriguing nucleic-acid-binding features of mammalian prion protein
Jerson L. Silva et al.
TRENDS IN BIOCHEMICAL SCIENCES (2008)
Curcumin binds to the α-helical intermediate and to the amyloid form of prion protein -: a new mechanism for the inhibition of PrPSc accumulation
Iva Hafner-Bratkovic et al.
JOURNAL OF NEUROCHEMISTRY (2008)
Molecular architecture of human prion protein amyloid:: A parallel, in-register β-structure
Nathan J. Cobb et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Scrapie infection of prion protein-deficient cell line upon ectopic expression of mutant prion proteins
Elke Maas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
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)
Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkage
Frederic Eghiaian et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Molecular mechanism for low pH triggered misfolding of the human prion protein
Mari L. DeMarco et al.
BIOCHEMISTRY (2007)
β-Sheet core of human prion protein amyloid fibrils as determined by hydrogen/deuterium exchange
Xiaojun Lu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Structural properties of prion protein protofibrils and fibrils: An experimental assessment of atomic models
Mari L. DeMarco et al.
BIOCHEMISTRY (2006)
Runaway domain swapping in amyloid-like fibrils of T7 endonuclease I
Zhefeng Guo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Elongated oligomers assemble into mammalian PrP amyloid fibrils
MH Tattum et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Amyloid formation by recombinant full-length prion proteins in phospholipid bicelle solutions
TT Lührs et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease
M Polymenidou et al.
LANCET NEUROLOGY (2005)
Amyloid-like fibrils of ribonuclease A with three-dimensional domain-swapped and native-like structure
S Sambashivan et al.
NATURE (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)
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)
Prion protein NMR structures of elk and of mouse/elk hybrids
AD Gossert et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
From conversion to aggregation: Protofibril formation of the prion protein
ML DeMarco et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Susceptibility of common fibroblast cell lines to transmissible spongiform encephalopathy agents
I Vorberg et al.
JOURNAL OF INFECTIOUS DISEASES (2004)
The tyrosine kinase inhibitor STI571 induces cellular clearance of PrPSc in prion-infected cells
A Ertmer et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Insight into the PrPC → PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants
F Eghiaian et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
MODIP revisited: re-evaluation and refinement of an automated procedure for modeling of disulfide bonds in proteins
VS Dani et al.
PROTEIN ENGINEERING (2003)
Intramolecular versus intermolecular disulfide bonds in prion proteins
E Welker et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Structural studies of the scrapie prion protein by electron crystallography
H Wille et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (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)
Three-dimensional domain swapping in the folded and molten-globule states of cystatins, an amyloid-forming structural superfamily
RA Staniforth et al.
EMBO JOURNAL (2001)
Crystal structure of the human prion protein reveals a mechanism for oligomerization
KJ Knaus et al.
NATURE STRUCTURAL BIOLOGY (2001)
Antibodies inhibit prion propagation and clear cell cultures of prion infectivity
D Peretz et al.
NATURE (2001)
NMR solution structure of the human prion protein
R Zahn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)