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We analyze the stability of micro-domains of ligand-receptor bonds that mediate the adhesion of biological model membranes.After evaluating the effects of membrane fluctuations on the binding affinity of a single bond, we characterize the organization of bonds within the domains by theoretical means.In a large range of parameters, we find the commonly suggested dense packing to be separated by a free energy barrier from a regime in which bonds are sparsely distributed.If bonds are mobile, a coexistence of the two regimes should emerge, which agrees with recent experimental observations.
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