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Solutes unmask differences in clustering versus phase separation of FET proteins.
Kar, Mrityunjoy; Vogel, Laura T; Chauhan, Gaurav; Felekyan, Suren; Ausserwöger, Hannes; Welsh, Timothy J; Dar, Furqan; Kamath, Anjana R; Knowles, Tuomas P J; Hyman, Anthony A; Seidel, Claus A M; Pappu, Rohit V.
Affiliation
  • Kar M; Max Planck Institute of Cell Biology and Genetics, 01307, Dresden, Germany.
  • Vogel LT; Department of Molecular Physical Chemistry, Heinrich Heine University, 40225, Düsseldorf, Germany.
  • Chauhan G; Department of Biomedical Engineering and Center for Biomolecular Condensates, Washington University in St. Louis, St. Louis, MO, 63130, USA.
  • Felekyan S; Department of Molecular Physical Chemistry, Heinrich Heine University, 40225, Düsseldorf, Germany.
  • Ausserwöger H; Centre for Misfolding Diseases, Yusuf Hamied Department of Chemistry, University of Cambridge, CB2 1EW, Cambridge, UK.
  • Welsh TJ; Centre for Misfolding Diseases, Yusuf Hamied Department of Chemistry, University of Cambridge, CB2 1EW, Cambridge, UK.
  • Dar F; Department of Biomedical Engineering and Center for Biomolecular Condensates, Washington University in St. Louis, St. Louis, MO, 63130, USA.
  • Kamath AR; Max Planck Institute of Cell Biology and Genetics, 01307, Dresden, Germany.
  • Knowles TPJ; Centre for Misfolding Diseases, Yusuf Hamied Department of Chemistry, University of Cambridge, CB2 1EW, Cambridge, UK.
  • Hyman AA; Max Planck Institute of Cell Biology and Genetics, 01307, Dresden, Germany. hyman@mpi-cbg.de.
  • Seidel CAM; Department of Molecular Physical Chemistry, Heinrich Heine University, 40225, Düsseldorf, Germany. cseidel@hhu.de.
  • Pappu RV; Department of Biomedical Engineering and Center for Biomolecular Condensates, Washington University in St. Louis, St. Louis, MO, 63130, USA. pappu@wustl.edu.
Nat Commun ; 15(1): 4408, 2024 May 23.
Article de En | MEDLINE | ID: mdl-38782886
ABSTRACT
Phase separation and percolation contribute to phase transitions of multivalent macromolecules. Contributions of percolation are evident through the viscoelasticity of condensates and through the formation of heterogeneous distributions of nano- and mesoscale pre-percolation clusters in sub-saturated solutions. Here, we show that clusters formed in sub-saturated solutions of FET (FUS-EWSR1-TAF15) proteins are affected differently by glutamate versus chloride. These differences on the nanoscale, gleaned using a suite of methods deployed across a wide range of protein concentrations, are prevalent and can be unmasked even though the driving forces for phase separation remain unchanged in glutamate versus chloride. Strikingly, differences in anion-mediated interactions that drive clustering saturate on the micron-scale. Beyond this length scale the system separates into coexisting phases. Overall, we find that sequence-encoded interactions, mediated by solution components, make synergistic and distinct contributions to the formation of pre-percolation clusters in sub-saturated solutions, and to the driving forces for phase separation.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Transition de phase Limites: Humans Langue: En Journal: Nat Commun Sujet du journal: BIOLOGIA / CIENCIA Année: 2024 Type de document: Article Pays d'affiliation: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Transition de phase Limites: Humans Langue: En Journal: Nat Commun Sujet du journal: BIOLOGIA / CIENCIA Année: 2024 Type de document: Article Pays d'affiliation: Allemagne
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