Abstract

Adhesion interactions mediated by multiple bond types are relevant for many biological and soft matter systems, including the adhesion of biological cells and functionalized colloidal particles to various substrates. To elucidate advantages and disadvantages of multiple bond populations for the stability of heterogeneous adhesion clusters of receptor-ligand pairs, a theoretical model for a homogeneous parallel adhesion bond cluster under constant loading is extended to several bond types. The stability of the entire cluster can be tuned by changing densities of different bond populations as well as their extensional rigidity and binding properties. In particular, bond extensional rigidities determine the distribution of total load to be shared between different sub-populations. Under a gradual increase of the total load, the rupture of a heterogeneous adhesion cluster can be thought of as a multistep discrete process, in which one of the bond sub-populations ruptures first, followed by similar rupture steps of other sub-populations or by immediate detachment of the remaining cluster. This rupture behavior is qualitatively independent of involved bond types, such as slip and catch bonds. Interestingly, an optimal stability is generally achieved when the total cluster load is shared such that loads on distinct bond populations are equal to their individual critical rupture forces. We also show that cluster heterogeneity can drastically affect cluster lifetime.

Highlights

  • Adhesion interactions via receptor-ligand bonds are essential for many biological and soft matter systems

  • We have investigated the stability of heterogeneous bond clusters under a constant load using the theoretical model for parallel-bond cluster

  • One of our main results from the mean-field approximation is that the rupture of heterogeneous bond clusters usually occurs as a multistep discrete process

Read more

Summary

Introduction

Adhesion interactions via receptor-ligand bonds are essential for many biological and soft matter systems. Examples include cell adhesion [1,2,3,4] and migration [5,6], synapse formation [7,8], adhesion of lipid vesicles [9,10,11] and drugdelivery carriers [12,13] to a substrate Such adhesive interactions depend on the properties of receptors and ligands (e.g., density, kinetic rates, mobility) and the characteristics of adhered particles (e.g., size, shape, deformability). Leukocytes before extravasation first bind to and roll at an endothelial cell layer, show a firm adhesion at the surface [19,20,21]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call