Light-Triggered Cargo Loading and Division of DNA-Containing Giant Unilamellar Lipid Vesicles

A minimal synthetic cell should contain a substrate for information storage and have the capability to divide. Notable efforts were made to assemble functional synthetic cells from the bottom up, however often lacking the capability to reproduce. Here, we develop a mechanism to fully control reversible cargo loading and division of DNA-containing giant unilamellar vesicles (GUVs) with light. We make use of the photosensitizer Chlorin e6 (Ce6) which self-assembles into lipid bilayers and leads to local lipid peroxidation upon illumination. On the time scale of minutes, illumination induces the formation of transient pores, which we exploit for cargo encapsulation or controlled release. In combination with osmosis, complete division of two daughter GUVs can be triggered within seconds of illumination due to a spontaneous curvature increase. We ultimately demonstrate the division of a selected DNA-containing GUV with full spatiotemporal control. proving the relevance of the division mechanism for bottom-up synthetic biology.

Automated summary

In this study, researchers successfully developed a new mechanism to control the division of DNA-containing giant unilamellar vesicles (GUVs) using a photosensitizer and osmosis. The research demonstrates the significance of this division mechanism for bottom-up synthetic biology.