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

Cappai, Roberto, Stewart, Leanne, Jobling, Michael F., Thyer, James M., White, Anthony R., Beyreuther, Konrad, Collins, Steven J., Masters, Colin L. and Barrow, Colin J. 1999, Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation, Biochemistry, vol. 38, no. 11, pp. 3280-3284, doi: 10.1021/bi982328z.

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Title Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation
Author(s) Cappai, Roberto
Stewart, Leanne
Jobling, Michael F.
Thyer, James M.
White, Anthony R.
Beyreuther, Konrad
Collins, Steven J.
Masters, Colin L.
Barrow, Colin J.ORCID iD for Barrow, Colin J. orcid.org/0000-0002-2153-7267
Journal name Biochemistry
Volume number 38
Issue number 11
Start page 3280
End page 3284
Total pages 5
Publisher American Chemical Society
Place of publication Washington, D.C.
Publication date 1999-03
ISSN 0006-2960
1520-4995
Keyword(s) 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
Language eng
DOI 10.1021/bi982328z
Field of Research 0601 Biochemistry And Cell Biology
1101 Medical Biochemistry And Metabolomics
0304 Medicinal And Biomolecular Chemistry
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©1999, American Chemical Society
Persistent URL http://hdl.handle.net/10536/DRO/DU:30099798

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