Phase separation of a yeast prion protein promotes cellular fitness

Author:

Franzmann Titus M.1ORCID,Jahnel Marcus12ORCID,Pozniakovsky Andrei1,Mahamid Julia3,Holehouse Alex S.4ORCID,Nüske Elisabeth1,Richter Doris1,Baumeister Wolfgang5,Grill Stephan W.12,Pappu Rohit V.4,Hyman Anthony A.1ORCID,Alberti Simon1ORCID

Affiliation:

1. Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.

2. Biotec, Technische Universität Dresden, Tatzberg 47/48, 01307 Dresden, Germany.

3. European Molecular Biology Laboratory, Heidelberg, Meyerhofstrasse 1, 69117 Heidelberg, Germany.

4. Department of Biomedical Engineering and Center for Biological Systems Engineering, Washington University in St. Louis, St. Louis, MO, USA.

5. Max Planck Institute of Biochemistry, Department of Molecular Structural Biology, Am Klopferspitz 18, 82152 Martinsried, Germany.

Abstract

Biophysical responses of proteins to stress Much recent work has focused on liquid-liquid phase separation as a cellular response to changing physicochemical conditions. Because phase separation responds critically to small changes in conditions such as pH, temperature, or salt, it is in principle an ideal way for a cell to measure and respond to changes in the environment. Small pH changes could, for instance, induce phase separation of compartments that store, protect, or inactivate proteins. Franzmann et al. used the yeast translation termination factor Sup35 as a model for a phase separation–induced stress response. Lowering the pH induced liquid-liquid phase separation of Sup35. The resulting liquid compartments subsequently hardened into gels, which sequestered the termination factor. Raising the pH triggered dissolution of the gels, concomitant with translation restart. Protecting Sup35 in gels could provide a fitness advantage to recovering yeast cells that must restart the translation machinery after stress. Science , this issue p. eaao5654

Funder

National Institutes of Health

Deutsche Forschungsgemeinschaft

Volkswagen Foundation

BMBF MaxSynBio

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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