Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease (Q48343268)

10 February 2018

title

Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease (English)

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10 February 2018

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8

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Marco Prinz

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object named as

Marco Prinz

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10 February 2018

author name string

Philipp Meier

1

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10 February 2018

Nicolas Genoud

2

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10 February 2018

Manuela Maissen

4

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10 February 2018

Thomas Rülicke

5

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10 February 2018

Andreas Zurbriggen

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10 February 2018

Alex J Raeber

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language of work or name

English

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publication date

1 April 2003

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10 February 2018

published in

Cell

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10 February 2018

volume

113

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10 February 2018

issue

1

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10 February 2018

page(s)

49-60

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10 February 2018

Prions and the immune system: a journey through gut, spleen, and nerves

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Mice devoid of PrP are resistant to scrapie

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The binding affinity of human IgG for its high affinity Fc receptor is determined by multiple amino acids in the CH2 domain and is modulated by the hinge region

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Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

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Binding of disease-associated prion protein to plasminogen.

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Prion protein is secreted in soluble forms in the epididymal fluid and proteolytically processed and transported in seminal plasma.

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Prevention of scrapie pathogenesis by transgenic expression of anti-prion protein antibodies

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Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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Efficient lymphoreticular prion propagation requires PrP(c) in stromal and hematopoietic cells.

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Complement facilitates early prion pathogenesis

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Cell-free formation of protease-resistant prion protein.

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Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

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Mechanism of scrapie replication

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Unusual topogenic sequence directs prion protein biogenesis

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Temporary inactivation of follicular dendritic cells delays neuroinvasion of scrapie

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Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie.

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Impaired prion replication in spleens of mice lacking functional follicular dendritic cells

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Measurement of the scrapie agent using an incubation time interval assay

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Attempts to restore scrapie prion infectivity after exposure to protein denaturants

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7 January 2021

Eight prion strains have PrP(Sc) molecules with different conformations

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7 January 2021

No propagation of prions in mice devoid of PrP.

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A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells

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A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies

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Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay

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Identifiers

DOI

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10 February 2018

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10 February 2018