Our laboratory investigates the principles that govern the formation, material properties, and biological functions of biomolecular condensates in cells. We study how phase separation organizes intracellular environments and regulates processes such as gene expression, RNA metabolism, and cellular stress responses through dynamic assemblies including paraspeckles, stress granules, and other RNA?protein condensates.
By integrating advanced live-cell imaging, quantitative image analysis, molecular and cell biology, and multi-omics approaches, we aim to understand how the biophysical properties of condensates influence cellular function and homeostasis.
We are also interested in how condensates can transition from liquid-like states to more solid-like assemblies, a process that can initiate protein aggregation during cellular stress or aging. Understanding these phase transitions is particularly important because aberrant condensate maturation is increasingly linked to neurodegenerative diseases, where dynamic RNA?protein assemblies can convert into pathological aggregates.
Ultimately, our goal is to uncover fundamental mechanisms connecting condensate biophysics with cellular function, aging, and disease.
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1. Imbalanced chromatin distribution in cellular senescence specifies paraspeckle dynamics. Gemone Biology. 2025 Sep. 26(1):264.
2. Reduced dynamicity and increased high-order protein assemblies in dense fibrillar component of the nucleolus under cellular senescence. Redox Biology 2024 Sep. 75:103279.
3. Ubiquitination of G3BP1 mediates stress granule disassembly in a context-specific manner. Science. 2021 Jun 372(6549):eabf6548.