One big challenge for the production of synthetic cells is that they must be able to divide to have offspring. In the journal Angewandte Chemie, a team from Heidelberg has now introduced a reproducible division mechanism for synthetic vesicles. It is based on osmosis and can be controlled by an enzymatic reaction or light.
Organisms cannot simply emerge from inanimate material ("abiogenesis"), cells always come from pre-existing cells. The prospect of synthetic cells newly built from the ground up is shifting this paradigm. However, one obstacle on this path is the question of controlled division--a requirement for having "progeny".
A team from the Max Planck Institute for Medical Research in Heidelberg, Heidelberg University, the Max Planck School Matter to Life, and Exzellenzcluster 3D Matter Made to Order, headed by Kerstin Göpfrich, has now reached a milestone by achieving complete control over the division of vesicles. To achieve this, they produced "gigantic unilamellar vesicles", which are micrometer-sized bubbles with a shell made of a lipid bilayer that resembles a natural membrane. A variety of lipids were combined to produce phase-separated vesicles--vesicles with membrane hemispheres that have different compositions. When the concentration of dissolved substances in the surrounding solution is increased, osmosis causes water to exit the vesicle through the membrane. This shrinks the volume of the vesicle while keeping the membrane surface equal. The resulting tension at the phase interface deforms the vesicles. They constrict themselves along their "equator"--increasingly with increasing osmotic pressure--until the two halves separate completely to form two (now single-phase) "daughter cells" with different membrane compositions. When the separation that occurs depends only on the concentration ratio of osmotically active particles (osmolarity) and is independent of the size of the vesicle.
The method by which the osmolarity is raised also plays no role. The methods used by the team included using a sucrose solution and adding an enzyme that splits glucose and fructose to slowly increase the concentration. Using light to initiate splitting of molecules in the solution gave the researchers complete spatial and temporal control over the separation. Using tightly controlled, local irradiation allowed the concentration to be increased selectively around a single vesicle, triggering it to selectively divide.
The team is also able to grow the single-phase cells back into phase-separated vesicles by fusing them with tiny vesicles that have the other type of membrane. This was made possible by attaching single strands of DNA to both different types of membrane. These bind to each other and bring the membranes of the daughter cell and the mini vesicle into very close contact so that they can fuse. The resulting gigantic vesicles can subsequently undergo further division cycles.
"Although these synthetic division mechanisms differ significantly from those of living cells," says Göpfrich, "the question arises of whether similar mechanisms played a role in the beginnings of life on earth or are involved in the formation of intracellular vesicles."
About the Author
Dr. Kerstin Goepfrich leads the research group Biophysical Engineering at the Max Planck Institute for Medical Research and in the Excellence Cluster 3D Matter Made to Order in Heidelberg. The physicist researches the assembly of artificial cells using novel tools such as DNA nanotechnology. As one of the founders of Ring-a-Scientist she is engaged in scientific communication.
Angewandte Chemie International Edition