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Tuning epithelial cell–cell adhesion and collective dynamics with functional DNA-E-Cadherin hybrid linkers

MPS-Authors
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Schoenit,  Andreas
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Lo Giudice,  Cristina
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Hahnen,  Nina
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Ollech,  Dirk
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Jahnke,  Kevin
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Göpfrich,  Kerstin
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Cavalcanti-Adam,  Elisabetta Ada
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Schoenit, A., Lo Giudice, C., Hahnen, N., Ollech, D., Jahnke, K., Göpfrich, K., et al. (2022). Tuning epithelial cell–cell adhesion and collective dynamics with functional DNA-E-Cadherin hybrid linkers. Nano Letters, 22(1), 302-310. doi:10.1021/acs.nanolett.1c03780.


Cite as: https://hdl.handle.net/21.11116/0000-0009-BCFA-A
Abstract
The binding strength between epithelial cells is crucial for tissue integrity, signal transduction and collective cell dynamics. However, there is no experimental approach to precisely modulate cell–cell adhesion strength at the cellular and molecular level. Here, we establish DNA nanotechnology as a tool to control cell–cell adhesion of epithelial cells. We designed a DNA-E-cadherin hybrid system consisting of complementary DNA strands covalently bound to a truncated E-cadherin with a modified extracellular domain. DNA sequence design allows to tune the DNA-E-cadherin hybrid molecular binding strength, while retaining its cytosolic interactions and downstream signaling capabilities. The DNA-E-cadherin hybrid facilitates strong and reversible cell–cell adhesion in E-cadherin deficient cells by forming mechanotransducive adherens junctions. We assess the direct influence of cell–cell adhesion strength on intracellular signaling and collective cell dynamics. This highlights the scope of DNA nanotechnology as a precision technology to study and engineer cell collectives.