2.2 Å Cryo-EM Tetra-Protofilament Structure of the Hamster Prion 108–144 Fibril Reveals an Ordered Water Channel in the Center

Location of the cross‐β structure in prion fibrils: A search by seeding and electron spin resonance spectroscopy

(2022) Brett K.‐Y. Chu et al.   PROTEIN SCIENCE

Structural basis for the helical filament formation of Escherichia coli glutamine synthetase

(2022) Pei‐Chi Huang et al.   PROTEIN SCIENCE

Aggregation Condition–Structure Relationship of Mouse Prion Protein Fibrils

(2021) Jēkabs Fridmanis et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Condition‐dependent structural collapse in the intrinsically disordered N‐terminal domain of prion protein

(2021) Eric H.‐L. Chen et al.   IUBMB LIFE

High-resolution structure and strain comparison of infectious mammalian prions

(2021) Allison Kraus et al.   MOLECULAR CELL

Amyloid structure determination in RELION-3.1

(2020) Sjors H. W. Scheres   Acta Crystallographica Section D-Structural Biology

Cryo-EM structure of a human prion fibril with a hydrophobic, protease-resistant core

(2020) Calina Glynn et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Cryo-EM structure of an amyloid fibril formed by full-length human prion protein

(2020) Li-Qiang Wang et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

UCSF ChimeraX : Structure visualization for researchers, educators, and developers

(2020) Eric F. Pettersen et al.   PROTEIN SCIENCE

Segments in the Amyloid Core that Distinguish Hamster from Mouse Prion Fibrils

(2019) Howard C.-H. Shen et al.   NEUROCHEMICAL RESEARCH

Macromolecular structure determination using X-rays, neutrons and electrons: recent developments in Phenix

(2019) Dorothee Liebschner et al.   Acta Crystallographica Section D-Structural Biology

Current Developments in Coot for Macromolecular Model Building of Electron Cryo‐microscopy and Crystallographic Data

(2019) Ana Casañal et al.   PROTEIN SCIENCE

Oriented chiral water wires in artificial transmembrane channels

(2018) Istvan Kocsis et al.   Science Advances

Helical reconstruction in RELION

(2017) Shaoda He et al.   JOURNAL OF STRUCTURAL BIOLOGY

MotionCor2: anisotropic correction of beam-induced motion for improved cryo-electron microscopy

(2017) Shawn Q Zheng et al.   NATURE METHODS

MolProbity: More and better reference data for improved all-atom structure validation

(2017) Christopher J. Williams et al.   PROTEIN SCIENCE

Species-dependent structural polymorphism of Y145Stop prion protein amyloid revealed by solid-state NMR spectroscopy

(2017) Theint Theint et al.   Nature Communications

Amyloid fibrils from the N-terminal prion protein fragment are infectious

(2016) Jin-Kyu Choi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The multivesicular body is the major internal site of prion conversion

(2015) Y.-I. Yim et al.   JOURNAL OF CELL SCIENCE

CTFFIND4: Fast and accurate defocus estimation from electron micrographs

(2015) Alexis Rohou et al.   JOURNAL OF STRUCTURAL BIOLOGY

Genetic Studies in Human Prion Diseases

(2014) Byung-Hoon Jeong et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

How do amino acid substitutions affect the amyloidogenic properties and seeding efficiency of prion peptides

(2013) Chi-Chen Chuang et al.   AMINO ACIDS

Genetics of prion diseases

(2013) Sarah E Lloyd et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Dissection of Conformational Conversion Events during Prion Amyloid Fibril Formation Using Hydrogen Exchange and Mass Spectrometry

(2013) Jogender Singh et al.   JOURNAL OF MOLECULAR BIOLOGY

Leu138 in bovine prion peptide fibrils is involved in seeding discrimination related to codon 129 M/V polymorphism in the prion peptide seeding experiment

(2011) Tai-Yan Liao et al.   FEBS Journal

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

(2010) Robert Tycko et al.   BIOCHEMISTRY

The genetics of prion diseases

(2010) James A Mastrianni   GENETICS IN MEDICINE

Dry amyloid fibril assembly in a yeast prion peptide is mediated by long-lived structures containing water wires

(2010) G. Reddy et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism

(2009) Matthew T Bishop et al.   BMC Medical Genetics

Distinct Structures of Scrapie Prion Protein (PrPSc)-seededVersusSpontaneous Recombinant Prion Protein Fibrils Revealed by Hydrogen/Deuterium Exchange

(2009) Vytautas Smirnovas et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductance

(2009) J. D. Ho et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Tuning the conformational properties of the prion peptide

(2008) Chai-Chi Ho et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS