Cytoskeletal elements,
like actin and myosin, have been reconstituted
inside lipid vesicles toward the vision to reconstruct cells from
the bottom up. Here, we realize the de novo assembly of entirely artificial
DNA-based cytoskeletons with programmed multifunctionality inside
synthetic cells. Giant unilamellar lipid vesicles (GUVs) serve as
cell-like compartments, in which the DNA cytoskeletons are repeatedly
and reversibly assembled and disassembled with light using the
cis
–
trans
isomerization of an azobenzene
moiety positioned in the DNA tiles. Importantly, we induced ordered
bundling of hundreds of DNA filaments into more rigid structures with
molecular crowders. We quantify and tune the persistence length of
the bundled filaments to achieve the formation of ring-like cortical
structures inside GUVs, resembling actin rings that form during cell
division. Additionally, we show that DNA filaments can be programmably
linked to the compartment periphery using cholesterol-tagged DNA as
a linker. The linker concentration determines the degree of the cortex-like
network formation, and we demonstrate that the DNA cortex-like network
can deform GUVs from within. All in all, this showcases the potential
of DNA nanotechnology to mimic the diverse functions of a cytoskeleton
in synthetic cells.