Adhesion plaque formation dynamics between polymer vesicles in the limit of highly concentrated binding sites

This work examines the process of adhesion plaque formation between pairs of copolymer vesicles presenting dense surface concentrations of avidin (NeutrAvidin) and biotin. Micropipet aspiration maintains constant membrane tension, as the low-tension vesicle membrane spreads over a second, more tense...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 23(2007), 13 vom: 19. Juni, Seite 7216-24
1. Verfasser: Nam, Jin (VerfasserIn)
Weitere Verfasser: Santore, Maria M
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, U.S. Gov't, Non-P.H.S. Membranes, Artificial Surface-Active Agents neutravidin Avidin 1405-69-2 Biotin 6SO6U10H04
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245 1 0 |a Adhesion plaque formation dynamics between polymer vesicles in the limit of highly concentrated binding sites 
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520 |a This work examines the process of adhesion plaque formation between pairs of copolymer vesicles presenting dense surface concentrations of avidin (NeutrAvidin) and biotin. Micropipet aspiration maintains constant membrane tension, as the low-tension vesicle membrane spreads over a second, more tensed vesicle. Spreading rates near 1 microm/s but as high as 7 microm/s (the adhesion plaque diameter) and contact angle growth rates of 2-14 deg/s are observed. The ultimate contact angles, in the range of 120-140 degrees, are independent of membrane tension and also exceed those previously reported. Adhesion plaque formation occurs in three phases: an initial step in which contact is established, typically lasting from a few seconds to a minute, an abrupt jump into contact in which both vesicles undergo substantial deformation, and a slower continued growth of the contact angle and area. Vesicle pairs are irreversibly bound at the plaque such that attempts to peel them apart cause membrane rupture at critical tensions as high as 4 mN/m, setting a lower bound on the interfacial strength. When the quantity tau(1 - cos theta) (with tau the membrane tension and theta the contact angle) is plotted as a function of time during plaque formation for different values of tau, the curves fail to collapse, indicating the chemical driving force for adhesion greatly exceeds the mechanical resisting tension 
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650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
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650 7 |a Biotin  |2 NLM 
650 7 |a 6SO6U10H04  |2 NLM 
700 1 |a Santore, Maria M  |e verfasserin  |4 aut 
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