Detection of the GPI-anchorless prion protein fragment PrP226 in human brain
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10189589" target="_blank" >RIV/00216208:11110/13:10189589 - isvavai.cz</a>
Alternative codes found
RIV/61389013:_____/13:00398156 RIV/00064190:_____/13:#0000663
Result on the web
<a href="http://dx.doi.org/10.1186/1471-2377-13-126" target="_blank" >http://dx.doi.org/10.1186/1471-2377-13-126</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/1471-2377-13-126" target="_blank" >10.1186/1471-2377-13-126</a>
Alternative languages
Result language
angličtina
Original language name
Detection of the GPI-anchorless prion protein fragment PrP226 in human brain
Original language description
Background: The accumulation of the misfolded forms of cellular prion protein, i.e. prions (PrPSc), in the brain is one of the crucial characteristics of fatal neurodegenerative disorders, called transmissible spongiform encephalopathies (TSEs). Cellularprion protein is normally linked to the cell surface by the glycosylphosphatidylinositol (GPI) anchor. There is accumulating evidence that the GPI-anchorless prion protein may act as an accelerator of formation and propagation of prions. In the TSE affected human brain we have previously discovered a novel GPI-anchorless prion protein fragment, named PrP226*, which ends with the tyrosine 226. This fragment can be labeled specifically by the monoclonal antibody V5B2. Methods: We developed a DELFIA basedassay for quick and sensitive detection of the PrP226* fragment in human brain tissue homogenates. By calculating the ratio between the signals of native (N) and denatured (D) samples applied to the assay we were able to observe signific
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EE - Microbiology, virology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
BMC Neurology
ISSN
1471-2377
e-ISSN
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Volume of the periodical
13
Issue of the periodical within the volume
September
Country of publishing house
GB - UNITED KINGDOM
Number of pages
12
Pages from-to
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UT code for WoS article
000324882600002
EID of the result in the Scopus database
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