Home > Publications Database > Live-cell quantification reveals viscoelastic regulation of synapsin condensates by α-synuclein. |
Journal Article | DZNE-2025-00540 |
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2025
Assoc.
Washington, DC [u.a.]
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Please use a persistent id in citations: doi:10.1126/sciadv.ads7627
Abstract: Synapsin and α-synuclein represent a growing list of condensate-forming proteins where the material states of condensates are directly linked to cellular functions (e.g., neurotransmission) and pathology (e.g., neurodegeneration). However, quantifying condensate material properties in living systems has been a substantial challenge. Here, we develop micropipette aspiration and whole-cell patch-clamp (MAPAC), a platform that allows direct material quantification of condensates in live cells. We find 10,000-fold variations in the viscoelasticity of synapsin condensates, regulated by the partitioning of α-synuclein, a marker for synucleinopathies. Through in vitro reconstitutions, we identify multiple molecular factors that distinctly regulate the viscosity, interfacial tension, and maturation of synapsin condensates, confirming the cellular roles of α-synuclein. Overall, our study provides unprecedented quantitative insights into the material properties of neuronal condensates and reveals a crucial role of α-synuclein in regulating condensate viscoelasticity. Furthermore, we envision MAPAC applicable to study a broad range of condensates in vivo.
Keyword(s): alpha-Synuclein: metabolism (MeSH) ; alpha-Synuclein: chemistry (MeSH) ; Viscosity (MeSH) ; Humans (MeSH) ; Synapsins: metabolism (MeSH) ; Synapsins: chemistry (MeSH) ; Elasticity (MeSH) ; Animals (MeSH) ; Biomolecular Condensates: metabolism (MeSH) ; Biomolecular Condensates: chemistry (MeSH) ; Patch-Clamp Techniques (MeSH) ; alpha-Synuclein ; Synapsins
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