Nanomaterial signatures program biomolecular condensates via triphasic separation for chemoplasticity remodeling

Membraneless organelles form by phase separation and regulate cell behavior. We show that cholesterol-patterned AuNPs program nanomaterial-induced stress granules (NSGs) by lowering G3BP1 condensation barriers through a solid-liquid-liquid triphasic sequence: nanomaterials recruit hnRNPC, which then engages G3BP1 to nucleate gel-like condensates. We map NSG microenvironments (temperature, polarity, pH, and proteasome activity), uncover dual disassembly-a slow VCP/19S-dependent route and a rapid SUMO/20S-dependent backup-and show that NSGs remodel chemo-plasticity: they mitigate doxorubicin/cisplatin toxicity in normal tissues yet sensitize tumors to nocodazole in vivo. Local induction and selective dissolution of NSGs thus offers a strategy to decouple efficacy from toxicity. Our results establish design rules linking nanomaterial surface chemistry to condensate programming and provide actionable levers to steer therapeutic outcomes.

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Publication Details

Journal
Nature Communications
Published
2025-10-29
DOI
https://doi.org/10.1038/s41467-025-64623-4
Citations
1
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.81
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article

Nanomaterial signatures program biomolecular condensates via triphasic separation for chemoplasticity remodeling

Zengshuai Yan, Yu‐qiang Ma, Liuting Zheng, Hong‐Ming Ding et al.
1 citations
Nature Communications
RNA Research and Splicing
0.81
article

Nanomaterial signatures program biomolecular condensates via triphasic separation for chemoplasticity remodeling

Zengshuai Yan, Yu‐qiang Ma, Liuting Zheng, Hong‐Ming Ding, Xiaoqi Tan, Yuxing Wang, Jin Chang, Da Huo, Xinyue Li, Qin Liu
article en
1 citations

Abstract

Membraneless organelles form by phase separation and regulate cell behavior. We show that cholesterol-patterned AuNPs program nanomaterial-induced stress granules (NSGs) by lowering G3BP1 condensation barriers through a solid-liquid-liquid triphasic sequence: nanomaterials recruit hnRNPC, which then engages G3BP1 to nucleate gel-like condensates. We map NSG microenvironments (temperature, polarity, pH, and proteasome activity), uncover dual disassembly-a slow VCP/19S-dependent route and a rapid SUMO/20S-dependent backup-and show that NSGs remodel chemo-plasticity: they mitigate doxorubicin/cisplatin toxicity in normal tissues yet sensitize tumors to nocodazole in vivo. Local induction and selective dissolution of NSGs thus offers a strategy to decouple efficacy from toxicity. Our results establish design rules linking nanomaterial surface chemistry to condensate programming and provide actionable levers to steer therapeutic outcomes.

Nature CommunicationsVol. 16(1)
China Pharmaceutical University (CN), Soochow University (CN), Nanjing Drum Tower Hospital (CN), Collaborative Innovation Center of Advanced Microstructures (CN), Nanjing Medical University (CN), Nanjing University (CN)
Openalex Percentile: Top 22%
RNA Research and Splicing
0.81
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