Researchers use high-speed atomic force microscopy to explore the binding mechanism of cadherins

NewsGuard 100/100 Score

Cell, tissue, and organ structure is maintained by cell-cell adhesion molecules that connect opposing cells. Cadherins are a class of essential cell-cell adhesion molecules for tissue formation and integrity, and defects in cadherin function cause various diseases (e.g., cancer invasion). Cadherin protrudes from the cell surface and binds another cadherin on an opposing cell to mediate cell-cell adhesion. The cadherin binding process mainly comprises two dimerization steps: X-dimer formation and strand-swap (SS-) dimer formation of the extracellular domains (ectodomains) of cadherin. However, interactions other than those involving the formation of the X- and SS-dimers have also been proposed, and the precise binding mechanism of cadherin remains controversial.

Shigetaka Nishiguchi of ExCELLS, Takayuki Uchihashi of ExCELLS and Nagoya University, and Tadaomi Furuta of Tokyo Tech applied high-speed atomic force microscopy (HS-AFM) to explore the binding mechanism of cadherins. HS-AFM can enable the visualization of single-molecule structures and dynamics in solution at the nanometer scale with sub-second time resolution by directly touching and scanning the surface of proteins through a sharp-tipped probe. HS-AFM revealed that cadherins existed as multiple dimeric structures, which based on their morphology may be classified as W-, cross-, and S-shaped dimers. Furthermore, the scientists conducted mutational and structural modeling analyses and found that W- and cross-shaped dimers corresponded to known SS-dimers and X-like dimers and that the S-shaped dimer is a novel conformation. The binding processes of cadherins directly visualized by HS-AFM also revealed that the dimerization process is completed within 1 second through conversion into the aforementioned three types of dimeric structures. Based on these HS-AFM observations, the scientists hypothesized that the binding mechanism progress through the sliding motion of the S-shaped dimer followed by the flipping motion of the X-dimer to form the SS-dimer, which is thought to be the final stable cadherin dimer.

To date, the binding mechanism of cadherins has been mainly investigated using structural analyses and cell and solution measurements, which can only analyze the binding states reflected by the large number of cadherins. The newly applied HS-AFM technique revealed the binding processes of individual cadherins at single-molecule resolution, which has not been achieved before. HS-AFM observation will pave the way for a deeper understanding of the binding mechanism of cadherins, which is important for tissue- and organ-level organization and cell-cell adhesion-related diseases.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Groundbreaking study advances human in vitro gametogenesis for infertility treatment