Proceedings of the National Academy of Sciences· 2026Q1
Trans - and cis -interaction dynamics of cadherin complexes on membranes visualized by high-speed atomic force microscopy
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- Q1SCImago
- 2026year
Short summary
High-speed atomic force microscopy visualized trans-strand-swap interactions through flipping and hopping motions and cis-interactions of cadherin complexes reconstituted on membranes, revealing dynamic and diverse conformations distinct from crystal structures.
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Key points
- High-speed atomic force microscopy was used to visualize cadherin complex dynamics on membranes.
- Trans-strand-swap interactions were observed through flipping and hopping motions.
- Cis-interactions were identified, contributing to multiple interaction patterns.
- Observed cadherin complex structures differed from those seen in crystal structures.
- Cadherins adopt dynamic and diverse conformations via multiple assembly pathways on membranes.
AI-generated from the title and abstract; the full text is not read.
Abstract
Classical cadherin-mediated cell–cell adhesion is important for maintaining the animal body and defects in adhesion cause severe diseases. The combination of trans - (between cells) and cis - (on the same membrane) interactions of the extracellular domains of cadherins is necessary for cadherin clustering in cell–cell junctions, which is essential for robust tissue formation. However, the solution structure and interaction dynamics of trans / cis -binding cadherin complexes have not been observed because of technical limitations; therefore, the cadherin clustering mechanism is not well understood. In this study, we reconstituted trans / cis -binding cadherin complexes on membranes and visualized their structure and dynamics using high-speed atomic force microscopy. Our method revealed trans -strand-swap interactions through flipping and hopping motions and cis -interactions, which contributed to multiple interaction patterns on the membrane. In addition, we observed cadherin complex structures that were distinct from those in crystal structures. These results suggest that cadherins adopt dynamic and diverse conformations through multiple assembly pathways on the membrane.
The authors' abstract, as published at the source. Proceedings of the National Academy of Sciences, 2026 · DOI ↗
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Field: Immunology and Allergy
Immunology and AllergyMedicine