Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation (Q59505876)

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7 November 2019

title

Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutation (English)

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7 November 2019

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2

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7 November 2019

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P Gambetti

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7 November 2019

author name string

N Singh

1

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7 November 2019

S G Chen

3

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7 November 2019

H Fujioka

4

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7 November 2019

S Richardson

5

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7 November 2019

R B Petersen

7

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language of work or name

English

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publication date

1 November 1997

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Journal of Biological Chemistry

7 November 2019

published in

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7 November 2019

volume

272

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7 November 2019

issue

45

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7 November 2019

page(s)

28461-28470

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7 November 2019

cites work

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Asparagine-linked glycosylation of the scrapie and cellular prion proteins

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

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Scrapie prion protein contains a phosphatidylinositol glycolipid

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Processing of a cellular prion protein: identification of N- and C-terminal cleavage sites.

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Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

21 January 2018

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Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

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Truncated forms of the human prion protein in normal brain and in prion diseases.

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A novel class of cell surface glycolipids of mammalian cells. Free glycosyl phosphatidylinositols

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Vectorial targeting of apical and basolateral plasma membrane proteins in a human adenocarcinoma epithelial cell line

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Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

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A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

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Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

21 January 2018

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Synthesis and trafficking of prion proteins in cultured cells

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Assembly of asparagine-linked oligosaccharides

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Bip/GRP78 but not calnexin associates with a precursor of glycosylphosphatidylinositol-anchored protein

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

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Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

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Role of microglia and host prion protein in neurotoxicity of a prion protein fragment.

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Mutant and infectious prion proteins display common biochemical properties in cultured cells.

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Proteins containing an uncleaved signal for glycophosphatidylinositol membrane anchor attachment are retained in a post-ER compartment

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Degradation of proteins within the endoplasmic reticulum

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How N-linked oligosaccharides affect glycoprotein folding in the endoplasmic reticulum

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Role of N-linked oligosaccharide recognition, glucose trimming, and calnexin in glycoprotein folding and quality control

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.272.45.28461

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9353306%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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