Adhesion of membranes via receptor–ligand complexes: Domain formation, binding cooperativity, and active processes
- 11 July 2009
- journal article
- review article
- Published by Royal Society of Chemistry (RSC) in Soft Matter
- Vol. 5 (17) , 3213-3224
Abstract
Cell membranes interact via anchored receptor and ligand molecules. Central questions on cell adhesion concern the binding affinity of these membrane-anchored molecules, the mechanisms leading to the receptor–ligand domains observed during adhesion, and the role of cytoskeletal and other active processes. In this review, these questions are addressed from a theoretical perspective. We focus on models in which the membranes are described as elastic sheets, and the receptors and ligands as anchored molecules. In these models, the thermal membrane roughness on the nanometre scale leads to a cooperative binding of anchored receptor and ligand molecules, since the receptor–ligand binding smoothens out the membranes and facilitates the formation of additional bonds. Patterns of receptor domains observed in Monte Carlo simulations point towards a joint role of spontaneous and active processes in cell adhesion. The interactions mediated by the receptors and ligand molecules can be characterized by effective membrane adhesion potentials that depend on the concentrations and binding energies of the molecules.Keywords
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This publication has 109 references indexed in Scilit:
- Spatiotemporal Regulation of T Cell Costimulation by TCR-CD28 Microclusters and Protein Kinase C θ TranslocationImmunity, 2008
- Force-induced growth of adhesion domains is controlled by receptor mobilityProceedings of the National Academy of Sciences, 2008
- A role for “self” in T-cell activationSeminars in Immunology, 2007
- T Cell Receptor-Proximal Signals Are Sustained in Peripheral Microclusters and Terminated in the Central Supramolecular Activation ClusterImmunity, 2006
- Newly generated T cell receptor microclusters initiate and sustain T cell activation by recruitment of Zap70 and SLP-76Nature Immunology, 2005
- Actin and agonist MHC–peptide complex–dependent T cell receptor microclusters as scaffolds for signalingJournal of Experimental Medicine, 2005
- Differential Segregation in a Cell-Cell Contact Interface: The Dynamics of the Immunological SynapseBiophysical Journal, 2002
- Direct observation of ligand recognition by T cellsNature, 2002
- T cell receptor ligation induces the formation of dynamically regulated signaling assembliesJournal of Cell Biology, 2002
- Synaptic pattern formation during cellular recognitionProceedings of the National Academy of Sciences, 2001