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Lysine/RNA-interactions drive and regulate biomolecular condensation.

Tina Ukmar-Godec | Saskia Hutten | Matthew P Grieshop | Nasrollah Rezaei-Ghaleh | Maria-Sol Cima-Omori | Jacek Biernat | Eckhard Mandelkow | Johannes Söding | Dorothee Dormann | Markus Zweckstetter
Nature communications | 2019

Cells form and use biomolecular condensates to execute biochemical reactions. The molecular properties of non-membrane-bound condensates are directly connected to the amino acid content of disordered protein regions. Lysine plays an important role in cellular function, but little is known about its role in biomolecular condensation. Here we show that protein disorder is abundant in protein/RNA granules and lysine is enriched in disordered regions of proteins in P-bodies compared to the entire human disordered proteome. Lysine-rich polypeptides phase separate into lysine/RNA-coacervates that are more dynamic and differ at the molecular level from arginine/RNA-coacervates. Consistent with the ability of lysine to drive phase separation, lysine-rich variants of the Alzheimer's disease-linked protein tau undergo coacervation with RNA in vitro and bind to stress granules in cells. Acetylation of lysine reverses liquid-liquid phase separation and reduces colocalization of tau with stress granules. Our study establishes lysine as an important regulator of cellular condensation.

Pubmed ID: 31266957

Research resources used in this publication

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Associated grants

  • Agency: EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council), International
    Id: 787679 - LLPS-NMR

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