TY - JOUR
T1 - Designer membraneless organelles sequester native factors for control of cell behavior
AU - Garabedian, Mikael V.
AU - Wang, Wentao
AU - Dabdoub, Jorge B.
AU - Tong, Michelle
AU - Caldwell, Reese M.
AU - Benman, William
AU - Schuster, Benjamin S.
AU - Deiters, Alexander
AU - Good, Matthew C.
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2021/9
Y1 - 2021/9
N2 - 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 90% of 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. [Figure not available: see fulltext.]
AB - 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 90% of 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. [Figure not available: see fulltext.]
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U2 - 10.1038/s41589-021-00840-4
DO - 10.1038/s41589-021-00840-4
M3 - Article
C2 - 34341589
AN - SCOPUS:85111874832
SN - 1552-4450
VL - 17
SP - 998
EP - 1007
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 9
ER -