期刊
ACS NANO
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c06125
关键词
membrane deformation; cell division; stomatocyte; dumbbell; FtsZ; Dynamin A
类别
资金
- BaSyC program of NWO-OCW
- ERC [883684]
- Novo Nordisk Foundation [NNF18SA0035142]
- INTERACTIONS, Marie Sklodowska-Curie Grant [847523]
- Marie Curie Actions (MSCA) [847523] Funding Source: Marie Curie Actions (MSCA)
The shape of cellular membranes determines their structure and function. A DNA-nanotechnology-based approach, called the synthetic membrane shaper (SMS), can stabilize the shape of cellular membranes and is compatible with protein reconstitution. This method provides a general tool for studying protein binding to complex membrane geometries.
Shape defines the structure and function of cellular membranes. In cell division, the cell membrane deforms into a dumbbell shape, while organdies such as the autophagosome exhibit stomatocyte shapes. Bottom-up in vitro reconstitution of protein machineries that stabilize or resolve the membrane necks in such deformed liposome structures is of considerable interest to characterize their function. Here we develop a DNA-nanotechnology-based approach that we call the synthetic membrane shaper (SMS), where cholesterol-linked DNA structures attach to the liposome membrane to reproducibly generate high yields of stomatocytes and dumbbells. In silico simulations confirm the shape-stabilizing role of the SMS. We show that the SMS is fully compatible with protein reconstitution by assembling bacterial divisome proteins (DynaminA, FtsZ:ZipA) at the catenoidal neck of these membrane structures. The SMS approach provides a general tool for studying protein binding to complex membrane geometries that will greatly benefit synthetic cell research.
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