Negatively charged α-synuclein condensate modulates partitioning of molecules

α-Synuclein (αSyn) aggregation via liquid-liquid phase separation (LLPS) has recently emerged as a crucial mechanism underlying amyloid fibril formation implicated in Parkinson's disease. However, comprehensive investigation of the physicochemical properties of αSyn condensate remains incomplete. Here, we demonstrate that αSyn condensates exhibit a highly negative electrostatic potential, revealed by preferential enrichment of positively charged fluorophores or fluorophore-labeled αSyn. We further demonstrate that αSyn LLPS is regulated by a balance between self-association and electrostatic repulsion, with excess negative charge inhibiting phase separation. To study αSyn LLPS in a cellular context, we generated a stably transfected SH-SY5Y cell line that forms gel-like, nontoxic αSyn condensates upon differentiation. Most importantly, these intracellular condensates maintain a negative electrostatic potential, as evidenced by mEGFP probes systematically engineered with increasing positive charge. Our findings underscore the central role of electrostatic potential in modulating molecular partitioning within αSyn condensates and suggest that similar electrostatic principles may apply to other biomolecular condensates.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-07-26
DOI
https://doi.org/10.1016/j.jbc.2025.110530
Citations
1
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
1.39

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article

Negatively charged α-synuclein condensate modulates partitioning of molecules

Leo Wong, S. R. Wayne Chen, Shuwen Chang, Qingqing Yang et al.
1 citations
Journal of Biological Chemistry
Parkinson's Disease Mechanisms and Treatments
1.39
article

Negatively charged α-synuclein condensate modulates partitioning of molecules

Leo Wong, S. R. Wayne Chen, Shuwen Chang, Qingqing Yang, Pengfei Zhang, Zhonghua Lu
article en
1 citations

Abstract

α-Synuclein (αSyn) aggregation via liquid-liquid phase separation (LLPS) has recently emerged as a crucial mechanism underlying amyloid fibril formation implicated in Parkinson's disease. However, comprehensive investigation of the physicochemical properties of αSyn condensate remains incomplete. Here, we demonstrate that αSyn condensates exhibit a highly negative electrostatic potential, revealed by preferential enrichment of positively charged fluorophores or fluorophore-labeled αSyn. We further demonstrate that αSyn LLPS is regulated by a balance between self-association and electrostatic repulsion, with excess negative charge inhibiting phase separation. To study αSyn LLPS in a cellular context, we generated a stably transfected SH-SY5Y cell line that forms gel-like, nontoxic αSyn condensates upon differentiation. Most importantly, these intracellular condensates maintain a negative electrostatic potential, as evidenced by mEGFP probes systematically engineered with increasing positive charge. Our findings underscore the central role of electrostatic potential in modulating molecular partitioning within αSyn condensates and suggest that similar electrostatic principles may apply to other biomolecular condensates.

Journal of Biological ChemistryVol. 301(9)
Chinese Academy of Sciences (CN), HKUST Shenzhen Research Institute (CN), Shenzhen Institute of Neuroscience (CN), Shenzhen Institutes of Advanced Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Parkinson's Disease Mechanisms and Treatments
1.39
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Negatively charged α-synuclein condensate modulates partitioning of molecules — Leo Wong, S. R. Wayne Chen, et al. · Journal of Biological Chemistry (2025) | TGRS Research Map | TGRS