Antagonist-induced deadhesion of specifically adhered vesicles

Ana Sunčana Smith, Barbara G. Lorz, Udo Seifert, Erich Sackmann

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

By use of a model system consisting of giant vesicles adhering to flat substrates, we identified, both experimentally and theoretically, two new control mechanisms for antagonist-induced deadhesion. Adhesion is established by specific binding of surface-grafted E-selectin and vesicle-carrying oligosaccharide LewisX. Deadhesion is achieved by controlled titration of monoclonal antibodies against E-selectin. The first mechanism is characterized by a considerable retraction of the contact zone resulting in a loss of contact area between the vesicle and the substrate. Within the developed theoretical framework, the observed equilibrium state is understood as a balance between the spreading pressure of the vesicle and the antagonist -induced lateral pressure at the edge of the contact zone. In the second mechanism, the antibodies induce unbinding by penetrating the contact zone without significantly affecting its size. This process reveals the decomposition of the adhesion zone into microdomains of tight binding separated by strongly fluctuating sections of the membrane. Both experiment and theory show a sigmoidal decrease of the number of bound ligands as a function of the logarithm of antagonist concentration. The work presented herein also provides a new method for the determination of the receptor binding affinity of either the surface-embedded ligands or the competing antagonist molecules.

Original languageEnglish
Pages (from-to)1064-1080
Number of pages17
JournalBiophysical Journal
Volume90
Issue number3
DOIs
StatePublished - Feb 2006
Externally publishedYes

Fingerprint

Dive into the research topics of 'Antagonist-induced deadhesion of specifically adhered vesicles'. Together they form a unique fingerprint.

Cite this