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Updated: Jun 19, 2025

Rapid In Vivo Fixation and Isolation of Translational Complexes from Eukaryotic Cells
Published on: December 25, 2021
Polysome collapse and RNA condensation fluidize the cytoplasm.
Ying Xie1, Tong Shu2, Tiewei Liu3
1Institute for Systems Genetics, New York University Langone Medical Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Cellular stress causes translation inhibition, leading to mRNA release and the formation of RNA-protein condensates. This process temporarily fluidizes the cytoplasm, aiding cellular stress responses and the formation of quality control bodies.
Area of Science:
- Cell Biology
- Biophysics
- Molecular Biology
Background:
- The crowded cellular environment impacts cell physiology.
- Cellular stress commonly inhibits translation, causing polysome collapse and mRNA release.
- Released mRNA forms ribonucleoprotein (RNP) condensates like stress granules.
Purpose of the Study:
- To investigate the biophysical changes in the cytoplasm during cellular stress.
- To elucidate the role of RNA condensation in cellular stress responses.
- To understand how cytoplasmic fluidity is modulated during stress.
Main Methods:
- Coarse-grained molecular dynamic simulations.
- Observation of polysome collapse and RNA condensation.
- Induction of synthetic RNA condensation using light.
Main Results:
- Polysome collapse and RNA condensation transiently fluidize the cytoplasm.
- Increased mesoscale diffusivity correlates with the formation of quality control bodies (Q-bodies).
- Synthetic RNA condensation also leads to cytoplasmic fluidization.
Conclusions:
- Stress-induced translation inhibition and RNP condensate formation modulate cytoplasmic physical properties.
- Cytoplasmic fluidization facilitates efficient cellular responses to stress.
- This mechanism enhances the formation of quality control bodies for misfolded peptide compartmentalization.
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