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Adhesion of membranes with competing specific and generic interactions

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TLDR
It is shown that the interplay of specific attractive and generic repulsive interactions can lead to the formation of a potential barrier which induces a line tension between bound and unbound membrane segments which results in lateral phase separation during adhesion.
Abstract
Biomimetic membranes in contact with a planar substrate or a second membrane are studied theoretically. The membranes contain specific adhesion molecules (stickers) which are attracted by the second surface. In the absence of stickers, the trans-interaction between the membrane and the second surface is assumed to be repulsive at short separations. It is shown that the interplay of specific attractive and generic repulsive interactions can lead to the formation of a potential barrier. This barrier induces a line tension between bound and unbound membrane segments which results in lateral phase separation during adhesion. The mechanism for adhesion-induced phase separation is rather general, as is demonstrated by considering two distinct cases involving: i) stickers with a linear attractive potential, and ii) stickers with a short-ranged square-well potential. In both cases, membrane fluctuations reduce the potential barrier and, therefore, decrease the tendency of phase separation.

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Journal ArticleDOI

Physics of cell adhesion: some lessons from cell-mimetic systems

TL;DR: The basic physical rules governing the physics of cell adhesion learned by studying cell-mimetic systems are reviewed and the importance of these rules in the context of cellular systems is demonstrated.
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Pattern formation during T-cell adhesion.

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Adhesion of membranes via receptor-ligand complexes: Domain formation, binding cooperativity, and active processes

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The formation of ordered nanoclusters controls cadherin anchoring to actin and cell–cell contact fluidity

TL;DR: This work shows that E-cadherins arrange in ordered clusters, providing the first demonstration of the existence of oligomeric cadherins at cell–cell contacts, and studies the consequences of the disruption of the cis-interface to show that it is not essential for adherens junction formation.
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Micropatterned "adherent/repellent" glass surfaces for studying the spreading kinetics of individual red blood cells onto protein-decorated substrates.

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