Phase separation provides a mechanism to reduce noise in cells.


Journal

Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511

Informations de publication

Date de publication:
24 01 2020
Historique:
received: 19 10 2018
revised: 18 09 2019
accepted: 06 12 2019
entrez: 25 1 2020
pubmed: 25 1 2020
medline: 22 4 2020
Statut: ppublish

Résumé

Expression of proteins inside cells is noisy, causing variability in protein concentration among identical cells. A central problem in cellular control is how cells cope with this inherent noise. Compartmentalization of proteins through phase separation has been suggested as a potential mechanism to reduce noise, but systematic studies to support this idea have been missing. In this study, we used a physical model that links noise in protein concentration to theory of phase separation to show that liquid droplets can effectively reduce noise. We provide experimental support for noise reduction by phase separation using engineered proteins that form liquid-like compartments in mammalian cells. Thus, phase separation can play an important role in biological signal processing and control.

Identifiants

pubmed: 31974256
pii: 367/6476/464
doi: 10.1126/science.aav6691
doi:

Substances chimiques

Bacterial Proteins 0
Luminescent Proteins 0
Recombinant Proteins 0
yellow fluorescent protein, Bacteria 0
DDX4 protein, human EC 3.6.1.-
DEAD-box RNA Helicases EC 3.6.4.13

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

464-468

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Auteurs

A Klosin (A)

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

F Oltsch (F)

Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Center for Systems Biology Dresden, 01307 Dresden, Germany.

T Harmon (T)

Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Max Planck Institute for the Physics of Complex Systems, 01187 Dresden Germany.

A Honigmann (A)

Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Cluster of Excellence Physics of Life, TU Dresden, 01062 Dresden, Germany.

F Jülicher (F)

Center for Systems Biology Dresden, 01307 Dresden, Germany. julicher@pks.mpg.de hyman@mpi-cbg.de zechner@mpi-cbg.de.
Max Planck Institute for the Physics of Complex Systems, 01187 Dresden Germany.
Cluster of Excellence Physics of Life, TU Dresden, 01062 Dresden, Germany.

A A Hyman (AA)

Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany. julicher@pks.mpg.de hyman@mpi-cbg.de zechner@mpi-cbg.de.
Center for Systems Biology Dresden, 01307 Dresden, Germany.
Cluster of Excellence Physics of Life, TU Dresden, 01062 Dresden, Germany.

C Zechner (C)

Max Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany. julicher@pks.mpg.de hyman@mpi-cbg.de zechner@mpi-cbg.de.
Center for Systems Biology Dresden, 01307 Dresden, Germany.
Cluster of Excellence Physics of Life, TU Dresden, 01062 Dresden, Germany.

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Classifications MeSH