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Single-Molecule Imaging Reveals Differential Stability of Alpha-Synuclein Aggregates

Wang, S.-C.; Zhang, S. J.; Gilboa, T.; Kang, J.; Kuzkina, A.; Kannarkat, G. T.; Chen, L.; Shih, W. M.; Chen-Plotkin, A. S.; Khurana, V.; Walt, D. R.

2026-07-04 neuroscience
10.64898/2026.06.30.735576 bioRxiv
Show abstract

Alpha-Synuclein (-syn) aggregation is central to Parkinson's disease (PD), yet measurements in biofluids are confounded by the coexistence of monomeric and aggregated species. Using Syn-IMAGR, a single-molecule imaging platform with sub-femtomolar sensitivity, we show that purified -syn aggregates undergo dilution-induced disassembly, revealing a concentration-dependent equilibrium. Applied to postmortem brain lysates, Syn-IMAGR distinguishes physiological -syn multimers, which are dimmer and readily dissociate upon dilution, from PD-associated aggregates, which remain detectable and exhibit greater structural resistance to disruption. These results indicate that -syn assemblies occupy distinct stability regimes, with PD-associated aggregates representing a more persistent and less dilution-sensitive structural state. Syn-IMAGR thus provides a quantitative framework for resolving -syn species and for probing their concentration-dependent equilibrium.

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