TABLE 1.
RT-QuIC | PMCA | |
Substrate | Recombinant PrP | Cellular form of PrP |
Protocol | Shaking/incubation | Sonication/incubation |
Measure of prion concentration | PrPSc seeding activity | PrPSc seeding activity |
Conversion products | Thioflavin T positive amyloid PrP | PrPSc assemblies |
Pros | -Real time and direct readout -Low biohazard -Detection in bodily fluids, notably CSF -CSF-based diagnostic for CJD -Commercial substrate available -Universal substrate -Good inter-laboratory reproducibility of the second-generation RT-QuIC -Use in other neurodegenerative diseases | -Generation of bona fide prion infectivity -Prion strain typing -Detection of sub-infectious prion doses -Detection in bodily fluids, notably blood -Correlation between infectivity and seeding activity in inactivation tests |
Cons | -Amplified product poorly infectious -Discrepancies between infectivity and seeding activity in inactivation tests | -Indirect readout (immunoblot) -No universal substrate -Strains refractory to amplification -Biohazardous method -No commercial substrate -Limited inter-laboratory reproducibility -Use of cofactors required for certain strains |
Application | Diagnostic | Research use |