NR AJUR
AU Race,R.E.; Caughey,B.W.; Graham,K.; Ernst,D.; Chesebro,B.
TI Analyses of frequency of infection, specific infectivity, and prion protein biosynthesis in scrapie-infected neuroblastoma cell clones
QU Journal of Virology 1988 Aug; 62(8): 2845-9
PT journal article
AB Scrapie, a spongiform encephalopathy of sheep and goats, is caused by a poorly understood transmissible agent in which no nucleic acid has been conclusively identified. Biochemical characterization of agent derived from animal tissues has not been precise because of the tenacious association of the agent with tissue components. As an approach toward obtaining homogeneous preparations of agent generated in vitro, we cloned scrapie-infected neuroblastoma cells. By frequency analysis, nearly every cell in expanded cultures contained scrapie agent. We also analyzed cell-dose infectivity relationships and developed a standard curve which allowed various cultures to be compared. Since a proteinase K (PK)-resistant form of a protein designated prion protein (PrP) has been found in partially purified preparations of scrapie agent from infected animal spleens and brains, we sought to identify this protein in cell cultures. No PK-resistant PrP was found in infected or uninfected cultures, although the PK-sensitive PrP was readily detected. These results suggested that PK-resistant PrP may not be an essential component of the infectious scrapie agent.
MH Animal; Endopeptidase K; Immunosorbent Techniques; Mice; Neuroblastoma; PrP 27-30 Protein; Prions/*pathogenicity; Scrapie/*etiology; Serine Endopeptidases/metabolism; Tumor Cells, Cultured; Viral Proteins/*biosynthesis/metabolism
AD Laboratory of Persistent Viral Diseases, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840.
SP englisch
PO USA