Calpain and other cytosolic proteases can contribute to the degradation of retro-translocated prion protein in the cytosol (Q40496138)

21 September 2017

Calpain and other cytosolic proteases can contribute to the degradation of retro-translocated prion protein in the cytosol (English)

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21 September 2017

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Xinhe Wang

1

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21 September 2017

Fei Wang

series ordinal

2

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21 September 2017

Man-Sun Sy

series ordinal

3

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21 September 2017

Jiyan Ma

series ordinal

4

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21 September 2017

language of work or name

English

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publication date

2 November 2004

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Journal of Biological Chemistry

21 September 2017

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21 September 2017

280

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21 September 2017

1

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21 September 2017

317-325

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https://api.crossref.org/works/10.1074%2FJBC.M410649200

21 September 2017

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Prion diseases of humans and animals: their causes and molecular basis

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M410649200

Prion protein and the transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Synthetic mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Recent advances in prion biology

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M410649200

Prion diseases: what is the neurotoxic molecule?

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M410649200

Normal host prion protein necessary for scrapie-induced neurotoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Prion protein expression in different species: analysis with a panel of new mAbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

A transmembrane form of the prion protein in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

De novo generation of a PrPSc-like conformation in living cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

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/10.1074%2FJBC.M410649200

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.M410649200

Biomedicine. A view from the top--prion diseases from 10,000 feet

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Cytosolic prion protein is not toxic and protects against Bax-mediated cell death in human primary neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Antitumor effect of an HER2-specific antibody-toxin fusion protein on human prostate cancer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Modulation of prion protein structural integrity by geldanamycin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Heterogeneity of normal prion protein in two- dimensional immunoblot: presence of various glycosylated and truncated forms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

More than folding: localized functions of cytosolic chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

NTera 2 cells: a human cell line which displays characteristics expected of a human committed neuronal progenitor cell

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Changes in the proteolytic activities of proteasomes and lysosomes in human fibroblasts produced by serum withdrawal, amino-acid deprivation and confluent conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Proteasome inhibitors: valuable new tools for cell biologists

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Disruption of heat shock factor 1 reveals an essential role in the ubiquitin proteolytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Retro-translocation of proteins from the endoplasmic reticulum into the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

A membrane protein required for dislocation of misfolded proteins from the ER

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

A membrane protein complex mediates retro-translocation from the ER lumen into the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Evolving questions and paradigm shifts in endoplasmic-reticulum-associated degradation (ERAD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

The calpain family and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Calpain-dependent endoproteolytic cleavage of PrPSc modulates scrapie prion propagation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M410649200

21 January 2018

Identifiers

DOI

10.1074/JBC.M410649200

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21 September 2017

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