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The Standard Scrapie Cell Assay: Development, Utility and Prospects

Prion diseases are a family of fatal neurodegenerative diseases that involve the misfolding of a host protein, PrP(C). Measuring prion infectivity is necessary for determining efficacy of a treatment or infectivity of a prion purification procedure; animal bioassays are, however, very expensive and...

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Detalles Bibliográficos
Autores principales: van der Merwe, Jacques, Aiken, Judd, Westaway, David, McKenzie, Debbie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306833/
https://www.ncbi.nlm.nih.gov/pubmed/25602372
http://dx.doi.org/10.3390/v7010180
Descripción
Sumario:Prion diseases are a family of fatal neurodegenerative diseases that involve the misfolding of a host protein, PrP(C). Measuring prion infectivity is necessary for determining efficacy of a treatment or infectivity of a prion purification procedure; animal bioassays are, however, very expensive and time consuming. The Standard Scrapie Cell Assay (SSCA) provides an alternative approach. The SSCA facilitates quantitative in vitro analysis of prion strains, titres and biological properties. Given its robust nature and potential for high throughput, the SSCA has substantial utility for in vitro characterization of prions and can be deployed in a number of settings. Here we provide an overview on establishing the SSCA, its use in studies of disease dissemination and pathogenesis, potential pitfalls and a number of remaining challenges.