(Q46897492)

26 December 2017

title

Copper (II) ions potently inhibit purified PrPres amplification (English)

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26 December 2017

4

Richard Kascsak

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26 December 2017

author name string

Nicholas R Orem

1

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26 December 2017

James C Geoghegan

2

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26 December 2017

Nathan R Deleault

3

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26 December 2017

Surachai Supattapone

5

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26 December 2017

language of work or name

English

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publication date

17 January 2006

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26 December 2017

Journal of Neurochemistry

published in

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26 December 2017

volume

96

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26 December 2017

issue

5

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26 December 2017

page(s)

1409-1415

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26 December 2017

Non-genetic propagation of strain-specific properties of scrapie prion protein.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Consequences of manganese replacement of copper for prion protein function and proteinase resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper coordination in the full-length, recombinant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

In vitro generation of infectious scrapie prions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Protease-resistant prion protein amplification reconstituted with partially purified substrates and synthetic polyanions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper binding to the octarepeats of the prion protein. Affinity, specificity, folding, and cooperativity: insights from circular dichroism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper binding to PrPC may inhibit prion disease propagation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Probing copper2+ binding to the prion protein using diamagnetic nickel2+ and 1H NMR: the unstructured N terminus facilitates the coordination of six copper2+ ions at physiological concentrations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Cell-free formation of protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Reversibility of scrapie inactivation is enhanced by copper.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper stimulates endocytosis of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Prion diseases: epidemiology in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Copper chelation delays the onset of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Metal imbalance and compromised antioxidant function are early changes in prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

Aberrant metal binding by prion protein in human prion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2006.03650.X

10.1111/J.1471-4159.2006.03650.X

21 January 2018

Identifiers

DOI

1 reference

26 December 2017

1 reference

26 December 2017