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Publication Date:
November 2005
ISSN:
1437-4315
DOI:
10.1515/BC.2005.131

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Editor-in-Chief: Brüne, Bernhard

Editorial Board Member: Ludwig, Stephan / Sies, Helmut / Stoffel, Markus / Turk, Boris / Wittinghofer, Alfred / Baumeister, Wolfgang / Bergeron, John / Bogyo, Matthew / Bürkle, Alexander / Cadenas, Enrique / Chiti, Fabrizio / Dikic, Ivan / Dobson, Christopher / Driessen, Arnold / Fritz, Hans / Gevaert, Kris / Hammann, Christian / Hartl, F. Ulrich / Häussinger, Dieter / Hiscott, John / Igarashi, Yasuyuki / Klotz, Lars-Oliver / Krüger, Achim / Magdolen, Viktor / Müschen, Markus / Narumiya, Shuh / Naumann, Michael / Pejler, Gunnar / Pfanner, Nikolaus / Pike, Robert / Potempa, Jan / Saftig, Paul / Sandhoff, Konrad / Schaffner, Walter / Sinning, Irmgard / Sommerhoff, Christian P.

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The polysaccharide scaffold of PrP 27-30 is a common compound of natural prions and consists of α-linked polyglucose

Christian Dumpitak1 / Michael Beekes2 / Nicole Weinmann3 / Sabine Metzger4 / Konstanze F. Winklhofer5 / Jörg Tatzelt6 / Detlev Riesner7

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Corresponding author

Citation Information: Biological Chemistry. Volume 386, Issue 11, Pages 1149–1155, ISSN (Online) 1437-4315, ISSN (Print) 1431-6730, DOI: 10.1515/BC.2005.131, November 2005

Publication History:
Received:
June 22, 2005
Accepted:
August 24, 2005
Published Online:
2005-11-24

Abstract

An inert polysaccharide scaffold identified as a 5–15% component of prion rods (PrP 27–30) is unambiguously distinguishable from the N-glycosyl groups and the GPI anchor of PrP, and consists predominantly of 1,4-linked glucose with some branching via 1,4,6-linked glucose. We show that this polysaccharide scaffold is a common secondary component of prions found in hamster full-length PrPSc, prion rods and in mouse ScN2a prions from cell culture. The preparation from prion rods was improved, resulting in a polysaccharide scaffold free of remaining infectivity. Furthermore, we determined the stereochemistry of the glycoside linkages as pre-dominantly if not entirely α-glycosidic. The origin of the polysaccharide, its interaction with PrP and its potential relation to glycogen and corpora amylacea are discussed.

Keywords: amyloid; corpora amylacea; glycogen; prion; scrapie; V-helix

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