Cell-free biogenesis of bacterial division proto-rings that can constrict liposomes

Journal Article (2020)
Author(s)

Elisa Godino (Kavli institute of nanoscience Delft, TU Delft - BN/Christophe Danelon Lab)

Jonás Noguera López (Kavli institute of nanoscience Delft, TU Delft - BN/Christophe Danelon Lab)

Ilias Zarguit (Kavli institute of nanoscience Delft, TU Delft - Education and Student Affairs)

Anne Doerr (Kavli institute of nanoscience Delft, TU Delft - BN/Technici en Analisten)

Mercedes Jimenez (CSIC - Centro de Investigaciones Biologicas (CIB))

Germán Rivas (CSIC - Centro de Investigaciones Biologicas (CIB))

Christophe Danelon (Kavli institute of nanoscience Delft, TU Delft - BN/Christophe Danelon Lab)

Research Group
BN/Christophe Danelon Lab
DOI related publication
https://doi.org/10.1038/s42003-020-01258-9
More Info
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Publication Year
2020
Language
English
Research Group
BN/Christophe Danelon Lab
Issue number
1
Volume number
3
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Abstract

A major challenge towards the realization of an autonomous synthetic cell resides in the encoding of a division machinery in a genetic programme. In the bacterial cell cycle, the assembly of cytoskeletal proteins into a ring defines the division site. At the onset of the formation of the Escherichia coli divisome, a proto-ring consisting of FtsZ and its membrane-recruiting proteins takes place. Here, we show that FtsA-FtsZ ring-like structures driven by cell-free gene expression can be reconstituted on planar membranes and inside liposome compartments. Such cytoskeletal structures are found to constrict the liposome, generating elongated membrane necks and budding vesicles. Additional expression of the FtsZ cross-linker protein ZapA yields more rigid FtsZ bundles that attach to the membrane but fail to produce budding spots or necks in liposomes. These results demonstrate that gene-directed protein synthesis and assembly of membrane-constricting FtsZ-rings can be combined in a liposome-based artificial cell.