Publication | Open Access
mTORC1 controls phase-separation and the biophysical properties of the cytoplasm by tuning crowding
12
Citations
67
References
2017
Year
Unknown Venue
Biophysical ModelingMolecular BiologyCytoskeletonCell BiophysicsProtein Phase SeparationAnalytical UltracentrifugationCellular PhysiologySingle Molecule BiophysicsStable Fluorescent ParticlesBioimagingMatrix BiologyMacromolecular AssembliesBiophysicsMtorc1 PathwayMacromolecular CrowdingCell DivisionBiopolymersCell BiologyBiomolecular ScienceBiophysical AspectBiomolecular EngineeringNatural SciencesExperimental BiophysicsBiophysical PropertiesMolecular BiophysicsCellular StructureCellular BiochemistryMedicine
Summary (Abstract) Macromolecular crowding has a profound impact on reaction rates and the physical properties of the cell interior, but the mechanisms that regulate crowding are poorly understood. We developed Genetically Encoded Multimeric nanoparticles (GEMs) to dissect these mechanisms. GEMs are homomultimeric scaffolds fused to a fluorescent protein. GEMs self-assemble into bright, stable fluorescent particles of defined size and shape. By combining tracking of GEMs with genetic and pharmacological approaches, we discovered that the mTORC1 pathway can tune the effective diffusion coefficient of macromolecules ≥15 nm in diameter more than 2-fold without any discernable effect on the motion of molecules ≥5 nm. These mTORCI-dependent changes in crowding and rheology affect phase-separation both in vitro and in vivo. Together, these results establish a role for mTORCI in controlling both the biophysical properties of the cytoplasm and the phase-separation of biopolymers.
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