Budding-driven localization of lipid domains at prescribed positions in confined giant unilamellar vesicles

04 January 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Giant unilamellar vesicles (GUVs) are widely used minimal cell models where essential biological features can be reproduced, isolated and studied. Although precise spatio-temporal distribution of membrane domains is a process of crucial importance in living cells, it is still highly challenging to generate anisotropic GUVs with domains at user-defined positions. Here we describe a novel and robust method to control the spatial position of lipid domains of liquid-ordered (Lo) / liquid-disordered (Ld) phase in giant unilamellar vesicles (GUVs). Our strategy consists in confining Lo/Ld phase-separated GUVs in microfluidic channels to define free budding regions where the minority phase lipid domains localize and grow by decreasing the line tension between the co-existing phases. We show that this process is governed by the respective fraction of the two phases, and not by the chemical nature of the lipids involved. The spatial position and number of domains are controlled by the design of the confining microchannel and could result in polarized GUVs with a controllable number of poles. The developed method is versatile and user-friendly, while allowing to perform multiple single-vesicle experiments in parallel.

Keywords

Synthetic cell
Giant vesicle
Microfluidics
Membrane phase separation
Lipid domain
GUV
Liposome

Supplementary materials

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Supporting Information PDF file
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This file includes: - Supplementary Figures S1-S5 - Legends of supplementary movies S1-S3
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Movie S1
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Time lapse fluorescence microscopy images displaying phase separation and maturation of lipid domains in Lo-rich GUVs. A left GUV corresponds to the one of Figure 2F (top). Images were recorded every 20 seconds for one hour. Scale bar: 50 µm.
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Movie S2
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Time lapse fluorescence microscopy images displaying phase separation and maturation of lipid domains in a Ld rich GUV from Figure 2F (bottom). Images were recorded every 20 seconds for one hour. Scale bar: 50 µm.
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Movie S3
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Time lapse fluorescence microscopy images displaying phase separation and maturation of lipid domains in a Ld rich GUV confined between pillars. Movie shows one example of formation of 4 Lo poles in GUVs. Images were recorded every 30 seconds for one hour. Scale bar: 50 µm.
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