Spatiotemporal control of coacervate formation within liposomes
Siddharth Deshpande,
Frank Brandenburg,
Anson Lau,
Mart G. F. Last,
Willem Kasper Spoelstra,
Louis Reese,
Sreekar Wunnava,
Marileen Dogterom and
Cees Dekker ()
Additional contact information
Siddharth Deshpande: Delft University of Technology
Frank Brandenburg: Delft University of Technology
Anson Lau: Delft University of Technology
Mart G. F. Last: Delft University of Technology
Willem Kasper Spoelstra: Delft University of Technology
Louis Reese: Delft University of Technology
Sreekar Wunnava: Delft University of Technology
Marileen Dogterom: Delft University of Technology
Cees Dekker: Delft University of Technology
Nature Communications, 2019, vol. 10, issue 1, 1-11
Abstract:
Abstract Liquid-liquid phase separation (LLPS), especially coacervation, plays a crucial role in cell biology, as it forms numerous membraneless organelles in cells. Coacervates play an indispensable role in regulating intracellular biochemistry, and their dysfunction is associated with several diseases. Understanding of the LLPS dynamics would greatly benefit from controlled in vitro assays that mimic cells. Here, we use a microfluidics-based methodology to form coacervates inside cell-sized (~10 µm) liposomes, allowing control over the dynamics. Protein-pore-mediated permeation of small molecules into liposomes triggers LLPS passively or via active mechanisms like enzymatic polymerization of nucleic acids. We demonstrate sequestration of proteins (FtsZ) and supramolecular assemblies (lipid vesicles), as well as the possibility to host metabolic reactions (β-galactosidase activity) inside coacervates. This coacervate-in-liposome platform provides a versatile tool to understand intracellular phase behavior, and these hybrid systems will allow engineering complex pathways to reconstitute cellular functions and facilitate bottom-up creation of synthetic cells.
Date: 2019
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DOI: 10.1038/s41467-019-09855-x
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