Material properties of phase-separated TFEB condensates regulate the autophagy-lysosome pathway

Author:

Wang Zheng1,Chen Di12,Guan Dongshi3ORCID,Liang Xiaobo24ORCID,Xue Jianfeng5,Zhao Hongyu1,Song Guangtao24,Lou Jizhong24ORCID,He Yan5,Zhang Hong12ORCID

Affiliation:

1. National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China

2. College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China

3. State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing, China

4. Key Laboratory of RNA Biology, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China

5. Department of Chemistry, Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology (Ministry of Education), Tsinghua University, Beijing, China

Abstract

Very little is known about how the material properties of protein condensates assembled via liquid–liquid phase separation (LLPS) are maintained and affect physiological functions. Here we show that liquid-like condensates of the transcription factor TFEB exhibit low fusion propensity in vitro and in living cells. We directly measured the attraction force between droplets, and we characterized the interfacial tension, viscosity, and elasticity of TFEB condensates. TFEB condensates contain rigid interfacial boundaries that govern their interaction behaviors. Several small molecules, including Ro-3306, modify the material properties of TFEB condensates, increasing their size and fusion propensity. These compounds promote lysosomal biogenesis and function in a TFEB-dependent manner without changing its cytoplasmic-nuclear translocation. Ro-3306 promotes autophagy activity, facilitating degradation of toxic protein aggregates. Our study helps explain how protein condensates are maintained as physically separate entities and reveals that the material properties of TFEB condensates can be harnessed to modulate TFEB activity.

Funder

Ministry of Science and Technology of the People’s Republic of China

Beijing Municipal Science and Technology Commission

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Rockefeller University Press

Subject

Cell Biology

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