Purpose |
Detecting misfolded αSyn |
Detecting misfolded αSyn |
Amplification mechanism |
Physical shaking (quaking) to induce protein aggregation |
Cycles of sonication and incubation to amplify aggregates |
Substrate |
Recombinant αSyn produced in vitro, highly purified |
Either recombinant αSyn or tissue-derived αSyn (e.g., from brain samples) |
Real-time detection |
Yes. Real-time monitoring based on ThT fluorescence |
No. Post-amplification detection such as immunoblotting is required |
Sensitivity |
High |
Extremely high |
Operational complexity |
Simple and suitable for high-throughput and fast detection |
Complex and time-consuming, often for research use |
Time |
Short, providing results rapidly |
Longer, requiring more time for amplification and analysis |
Clinical application |
Common in clinical diagnostics, fast and efficient |
Less commonly used in clinical settings, mainly for research purpose |
Safety |
Simple and safe, with lower biological hazard |
More complex handling with additional experimental steps |