(Q46591995)

23 December 2017

title

Assembly of natural and recombinant prion protein into fibrils (English)

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23 December 2017

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2

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23 December 2017

Stanley B. Prusiner

5

object named as

Stanley B Prusiner

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23 December 2017

Karl-Werner Leffers

1

1 reference

23 December 2017

Jan Stöhr

3

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23 December 2017

Erika Junger

4

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23 December 2017

Detlev Riesner

6

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23 December 2017

publication date

1 June 2005

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23 December 2017

published in

Biological Chemistry

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23 December 2017

volume

386

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23 December 2017

issue

6

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23 December 2017

page(s)

569-580

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23 December 2017

Atypical effect of salts on the thermodynamic stability of human prion protein

cites work

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Prion rods contain an inert polysaccharide scaffold

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Effect of glycosylphosphatidylinositol anchor-dependent and -independent prion protein association with model raft membranes on conversion to the protease-resistant isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Folding of prion protein to its native alpha-helical conformation is under kinetic control

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Pathway complexity of prion protein assembly into amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Protofibrils, pores, fibrils, and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Pathologic conformations of prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

RNA molecules stimulate prion protein conversion

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Neurotoxicity of a prion protein fragment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

16 Solubilization of functional membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Scrapie: a modified membrane hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Structural intermediates in the putative pathway from the cellular prion protein to the pathogenic form.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Infection specific prion protein (PrP) accumulates on neuronal plasmalemma in scrapie infected mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Murine scrapie-infected neurons in vivo release excess prion protein into the extracellular space

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Protein-only transmission of three yeast prion strains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Prion rods contain small amounts of two host sphingolipids as revealed by thin-layer chromatography and mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Cell-free formation of protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

The structural transition of the prion protein into its pathogenic conformation is induced by unmasking hydrophobic sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Synthetic mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

In vitro amplification of protease-resistant prion protein requires free sulfhydryl groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Amyloid aggregates of the HET-s prion protein are infectious

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Identification of a common sphingolipid-binding domain in Alzheimer, prion, and HIV-1 proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Purification and properties of the cellular prion protein from Syrian hamster brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

A change in the conformation of prions accompanies the emergence of a new prion strain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Attempts to restore scrapie prion infectivity after exposure to protein denaturants

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Amyloid fibrillogenesis: themes and variations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Eight prion strains have PrP(Sc) molecules with different conformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Binding of prion protein to lipid membranes and implications for prion conversion

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Unfolding the role of protein misfolding in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Evidence for the prion hypothesis: induction of the yeast [PSI+] factor by in vitro- converted Sup35 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Identification of two prion protein regions that modify scrapie incubation time

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Conformational variations in an infectious protein determine prion strain differences

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Mutant PrPSc conformers induced by a synthetic peptide and several prion strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Scrapie infectivity is independent of amyloid staining properties of the N-terminally truncated prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Structural studies of the scrapie prion protein by electron crystallography

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Sphingolipid Depletion Increases Formation of the Scrapie Prion Protein in Neuroblastoma Cells Infected with Prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2005.067

Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis

21 January 2018

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1515/BC.2005.067

Protease-resistant prion protein produced in vitro lacks detectable infectivity.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1515/BC.2005.067

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1515/BC.2005.067

Propagation of prion strains through specific conformers of the prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1515/BC.2005.067

Identifiers

DOI

10.1515/BC.2005.067

1 reference

23 December 2017

PubMed ID

16006244

1 reference

23 December 2017