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Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior

Subcellular compartmentalization of macromolecules increases flux and prevents inhibitory interactions to control biochemical reactions. Inspired by this functionality, we sought to build designer compartments that function as hubs to regulate the flow of information through cellular control systems...

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Autores principales: Garabedian, Mikael V., Wang, Wentao, Dabdoub, Jorge B., Tong, Michelle, Caldwell, Reese M., Benman, William, Schuster, Benjamin S., Deiters, Alexander, Good, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387445/
https://www.ncbi.nlm.nih.gov/pubmed/34341589
http://dx.doi.org/10.1038/s41589-021-00840-4
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author Garabedian, Mikael V.
Wang, Wentao
Dabdoub, Jorge B.
Tong, Michelle
Caldwell, Reese M.
Benman, William
Schuster, Benjamin S.
Deiters, Alexander
Good, Matthew C.
author_facet Garabedian, Mikael V.
Wang, Wentao
Dabdoub, Jorge B.
Tong, Michelle
Caldwell, Reese M.
Benman, William
Schuster, Benjamin S.
Deiters, Alexander
Good, Matthew C.
author_sort Garabedian, Mikael V.
collection PubMed
description Subcellular compartmentalization of macromolecules increases flux and prevents inhibitory interactions to control biochemical reactions. Inspired by this functionality, we sought to build designer compartments that function as hubs to regulate the flow of information through cellular control systems. We report a synthetic membraneless organelle platform to control endogenous cellular activities through sequestration and insulation of native proteins. We engineer and express a disordered protein scaffold to assemble micron size condensates and recruit endogenous clients via genomic tagging with high-affinity dimerization motifs. By relocalizing up to ninety percent of a targeted enzymes to synthetic condensates, we efficiently control cellular behaviors, including proliferation, division, and cytoskeletal organization. Further, we demonstrate multiple strategies for controlled cargo release from condensates to switch cells between functional states. These synthetic organelles offer a powerful and generalizable approach to modularly control cell decision-making in a variety of model systems with broad applications for cellular engineering.
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spelling pubmed-83874452022-02-02 Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior Garabedian, Mikael V. Wang, Wentao Dabdoub, Jorge B. Tong, Michelle Caldwell, Reese M. Benman, William Schuster, Benjamin S. Deiters, Alexander Good, Matthew C. Nat Chem Biol Article Subcellular compartmentalization of macromolecules increases flux and prevents inhibitory interactions to control biochemical reactions. Inspired by this functionality, we sought to build designer compartments that function as hubs to regulate the flow of information through cellular control systems. We report a synthetic membraneless organelle platform to control endogenous cellular activities through sequestration and insulation of native proteins. We engineer and express a disordered protein scaffold to assemble micron size condensates and recruit endogenous clients via genomic tagging with high-affinity dimerization motifs. By relocalizing up to ninety percent of a targeted enzymes to synthetic condensates, we efficiently control cellular behaviors, including proliferation, division, and cytoskeletal organization. Further, we demonstrate multiple strategies for controlled cargo release from condensates to switch cells between functional states. These synthetic organelles offer a powerful and generalizable approach to modularly control cell decision-making in a variety of model systems with broad applications for cellular engineering. 2021-08-02 2021-09 /pmc/articles/PMC8387445/ /pubmed/34341589 http://dx.doi.org/10.1038/s41589-021-00840-4 Text en https://www.springernature.com/gp/open-research/policies/accepted-manuscript-termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Garabedian, Mikael V.
Wang, Wentao
Dabdoub, Jorge B.
Tong, Michelle
Caldwell, Reese M.
Benman, William
Schuster, Benjamin S.
Deiters, Alexander
Good, Matthew C.
Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title_full Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title_fullStr Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title_full_unstemmed Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title_short Designer Membraneless Organelles Sequester Native Factors for Control of Cell Behavior
title_sort designer membraneless organelles sequester native factors for control of cell behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387445/
https://www.ncbi.nlm.nih.gov/pubmed/34341589
http://dx.doi.org/10.1038/s41589-021-00840-4
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