Evidence map›Paper›PMID 34939414›Full record

ArticleNano letters2022

Tuning Epithelial Cell-Cell Adhesion and Collective Dynamics with Functional DNA-E-Cadherin Hybrid Linkers.

Andreas Schoenit, Cristina Lo Giudice, Nina Hahnen, Dirk Ollech, Kevin Jahnke, Kerstin Göpfrich, Elisabetta Ada Cavalcanti-Adam

Open access · hybridAbstract read
In one paragraph

Article in Nano letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Membrane-Associated Biomolecules for Synthetic Cell Signalling.Chembiochem : a European journal of chemical biology · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Quantitative Super-Resolution Imaging of Molecular Tension.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Article
  8. Bottom-up synthetic immunology.Nature nanotechnology · 2024
    Review
  9. Engineering tunable catch bonds with DNA.Nature communications · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Andreas SchoenitBiophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.
Cristina Lo GiudiceDepartment of Cellular Biophysics, Growth Factor Mechanobiology Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.
Nina HahnenBiophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.
Dirk OllechDepartment of Cellular Biophysics, Growth Factor Mechanobiology Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.
Kevin JahnkeBiophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.
Kerstin GöpfrichBiophysical Engineering Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.ORCID 0000-0003-2115-3551
Elisabetta Ada Cavalcanti-AdamDepartment of Cellular Biophysics, Growth Factor Mechanobiology Group, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120 Heidelberg, Germany.ORCID 0000-0003-0243-1552
Max Planck Institute for Medical Research · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Adherens JunctionsCadherinsCell AdhesionDNAEpithelial CellsCadherinsDNAadherens junctioncell−cell adhesion strengthcollective migrationDNA nanotechnologyDNA−protein hybridE-cadherinepithelial cellsmechanotransduction

Identifiers

PMID34939414
PMCPMC8759084
OpenAlexW4220736109

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.