Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: Implications for the mechanism of prion formation

Biochemistry

Volumn 38, Issue 11, 1999, Pages 3280-3284

  Cappai, Roberto ^a   Stewart, Leanne ^a   Jobling, Michael F ^a   Thyer, James M ^a   White, Anthony R ^a   Beyreuther, Konrad ^b   Collins, Steven J ^a   Masters, Colin L ^a   Barrow, Colin J ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

^b UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

ALPHA HELIX; ANIMAL CELL; ARTICLE; BRAIN SPONGIOSIS; CIRCULAR DICHROISM; DISULFIDE BOND; GENE CONVERSION; GENE MUTATION; LIGAND BINDING; MOUSE; NERVE DEGENERATION; NONHUMAN; PRION DISEASE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN EXPRESSION; PROTEIN SECONDARY STRUCTURE;

AMINO ACID SUBSTITUTION; ANIMALS; CIRCULAR DICHROISM; DRUG RESISTANCE; ENDOPEPTIDASE K; ESCHERICHIA COLI; LEUCINE; MICE; MICE, INBRED BALB C; PRION DISEASES; PRIONS; PROLINE; PROTEIN STRUCTURE, SECONDARY; RECOMBINANT PROTEINS;

EID: 0033574264     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi982328z     Document Type: Article

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