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Mechanochemical signal transduction in synthetic cells

View ORCID ProfileKevin Jahnke, View ORCID ProfileMaja Illig, Marlene Scheffold, Mai P. Tran, Ulrike Mersdorf, View ORCID ProfileKerstin Göpfrich
doi: https://doi.org/10.1101/2022.04.26.489423
Kevin Jahnke
1Biophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
2Department of Physics and Astronomy, Heidelberg University, D-69120 Heidelberg, Germany
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Maja Illig
1Biophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
2Department of Physics and Astronomy, Heidelberg University, D-69120 Heidelberg, Germany
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Marlene Scheffold
1Biophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
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Mai P. Tran
1Biophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
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Ulrike Mersdorf
3Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
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Kerstin Göpfrich
1Biophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany
2Department of Physics and Astronomy, Heidelberg University, D-69120 Heidelberg, Germany
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Abstract

Mechanotransduction determines the adaptive response of natural cells via transmem-brane proteins1. The incorporation of membrane-spanning structures to guide cellular function and to enable transmembrane signalling is therefore a critical aim for bottom-up synthetic biology2,3,4. Here, we design membrane-spanning DNA origami signalling units (DOSUs) and mechanically couple them to DNA cytoskeletons5 encapsulated within giant unilamellar vesicles (GUVs). We verify the assembly and incorporation of the DOSUs into the GUV membranes and achieve their clustering upon external stimulation. The transmembrane-spanning DOSUs act as a pore to allow for the transport of single-stranded DNA into the GUVs. We employ this to externally trigger the reconfiguration of DNA cytoskeletons within GUVs using strand displacement reactions. In addition to chemical signalling, we achieve the mechanical coupling of the externally added DOSUs and the internal DNA cytoskeletons. We induce clustering of the DOSUs, which triggers a symmetry break in the organization of the DNA cytoskeleton which is mechanically coupled to the DOSU.Our work thus provides a mechanical and chemical transmembrane signaling module towards the assembly of stimuli-responsive and adaptive synthetic cells.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted April 26, 2022.
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Mechanochemical signal transduction in synthetic cells
Kevin Jahnke, Maja Illig, Marlene Scheffold, Mai P. Tran, Ulrike Mersdorf, Kerstin Göpfrich
bioRxiv 2022.04.26.489423; doi: https://doi.org/10.1101/2022.04.26.489423
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Mechanochemical signal transduction in synthetic cells
Kevin Jahnke, Maja Illig, Marlene Scheffold, Mai P. Tran, Ulrike Mersdorf, Kerstin Göpfrich
bioRxiv 2022.04.26.489423; doi: https://doi.org/10.1101/2022.04.26.489423

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