Intracellular accumulation of a 46 kDa species of mouse prion protein as a result of loss of glycosylation in cultured mammalian cells

Biochemical and Biophysical Research Communications

Volumn 349, Issue 1, 2006, Pages 153-161

  Biswas, Subhabrata ^a   Langeveld, Jan P M ^b   Tipper, Donald ^a   Lu, Shan ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^b WAGENINGEN UNIVERSITY   (Netherlands)

Author keywords

Dimerization; Glycosylation; Prion

Indexed keywords

CELL PROTEIN; CYTOPLASM PROTEIN; GLYCOSYLPHOSPHATIDYLINOSITOL; ISOPROTEIN; MURINE PRION PROTEIN; MUTANT PROTEIN; POLYCLONAL ANTISERUM; PRION PROTEIN; PROTEIN P46; SIGNAL PEPTIDE; TUNICAMYCIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL CULTURE; CELLULAR DISTRIBUTION; CROSS REACTION; DEGENERATIVE DISEASE; DEGLYCOSYLATION; DIMERIZATION; DISEASE PREDISPOSITION; GOLGI COMPLEX; HUMAN; HUMAN CELL; MOLECULAR WEIGHT; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRION DISEASE; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; PROTEIN LOCALIZATION;

ANIMALS; BRAIN; CELLS, CULTURED; CYTOPLASM; DIMERIZATION; GENETIC PREDISPOSITION TO DISEASE; GLYCOSYLATION; GOLGI APPARATUS; HUMANS; MICE; PRION DISEASES; PRIONS; PROTEIN STRUCTURE, TERTIARY;

MAMMALIA; MURINAE; ORYCTOLAGUS CUNICULUS;

EID: 33748329580     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.08.035     Document Type: Article

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