(Q51825374)

13 April 2018

title

Ionic strength and transition metals control PrPSc protease resistance and conversion-inducing activity. (English)

1 reference

13 April 2018

1 reference

Koren Nishina

1

1 reference

13 April 2018

Samantha Jenks

series ordinal

2

1 reference

13 April 2018

Surachai Supattapone

series ordinal

3

1 reference

13 April 2018

language of work or name

English

0 references

publication date

19 July 2004

1 reference

13 April 2018

Journal of Biological Chemistry

published in

1 reference

13 April 2018

volume

279

1 reference

13 April 2018

issue

39

1 reference

13 April 2018

page(s)

40788-40794

1 reference

13 April 2018

Novel proteinaceous infectious particles cause scrapie

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Interactions between prion protein isoforms: the kiss of death?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Prion research: the next frontiers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Identification of a protein that purifies with the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

A protease-resistant protein is a structural component of the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Separation of scrapie prion infectivity from PrP amyloid polymers

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper chelation delays the onset of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Reversibility of scrapie inactivation is enhanced by copper

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

In vitro prion protein conversion in detergent-solubilized membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Strain-specified relative conformational stability of the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Branched polyamines cure prion-infected neuroblastoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Location and properties of metal-binding sites on the human prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper binding to the prion protein: structural implications of four identical cooperative binding sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Raman spectroscopic study on the copper(II) binding mode of prion octapeptide and its pH dependence

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

XAFS study of the high-affinity copper-binding site of human PrP(91-231) and its low-resolution structure in solution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Mapping Cu(II) binding sites in prion proteins by diethyl pyrocarbonate modification and matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometric footprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Electron paramagnetic resonance evidence for binding of Cu(2+) to the C-terminal domain of the murine prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Molecular characteristics of the major scrapie prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

The role of disulfide bridge in the folding and stability of the recombinant human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

On the mechanism of alpha-helix to beta-sheet transition in the recombinant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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/10.1074%2FJBC.M406548200

Scrapie agent contains a hydrophobic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Functional interactions of nucleocapsid protein of feline immunodeficiency virus and cellular prion protein with the viral RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

The prion protein has RNA binding and chaperoning properties characteristic of nucleocapsid protein NCP7 of HIV-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

The prion protein has DNA strand transfer properties similar to retroviral nucleocapsid protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Prion-protein-specific aptamer reduces PrPSc formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Concentration and removal of prion proteins from biological solutions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

DNA-induced partial unfolding of prion protein leads to its polymerisation to amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Small, highly structured RNAs participate in the conversion of human recombinant PrP(Sen) to PrP(Res) in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

RNA molecules stimulate prion protein conversion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Reconstitution of prion infectivity from solubilized protease-resistant PrP and nonprotein components of prion rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Cellular heparan sulfate participates in the metabolism of prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Identification of the heparan sulfate binding sites in the cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Binding of disease-associated prion protein to plasminogen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Actin and actin-binding proteins. A critical evaluation of mechanisms and functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

The metallobiology of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Misfolded CuZnSOD and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Dramatic aggregation of Alzheimer abeta by Cu(II) is induced by conditions representing physiological acidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Rapid induction of Alzheimer A beta amyloid formation by zinc.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper binding to the PrP isoforms: a putative marker of their conformation and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Zinc-induced Alzheimer's Abeta1-40 aggregation is mediated by conformational factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Aberrant metal binding by prion protein in human prion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Ecosystems supporting clusters of sporadic TSEs demonstrate excesses of the radical-generating divalent cation manganese and deficiencies of antioxidant co factors Cu, Se, Fe, Zn. Does a foreign cation substitution at prion protein's Cu domain initi

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper and zinc binding modulates the aggregation and neurotoxic properties of the prion peptide PrP106-126.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper converts the cellular prion protein into a protease-resistant species that is distinct from the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper refolding of prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Ablation of the metal ion-induced endocytosis of the prion protein by disease-associated mutation of the octarepeat region

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Copper stimulates endocytosis of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Normal prion protein has an activity like that of superoxide dismutase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

The chemistry of scrapie infection: implications of the 'ice 9' metaphor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Structural clues to prion replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Reversibility of scrapie-associated prion protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

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/10.1074%2FJBC.M406548200

Clinical and pathological features and laboratory confirmation of Creutzfeldt-Jakob disease in a recipient of pituitary-derived human growth hormone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Proteolytic inactivation of the bovine spongiform encephalopathy agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

Strain-specific prion-protein conformation determined by metal ions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M406548200

21 January 2018

Identifiers

DOI

10.1074/JBC.M406548200

1 reference

13 April 2018

1 reference

13 April 2018