Abstract
Selective binding of multivalent ligands within a mixture of polyvalent amphiphiles provides, in principle, a simple mechanism for driving domain formation in self-assemblies. Divalent cations are shown here to crossbridge polyanionic amphiphiles, which thereby demix from neutral amphiphiles and form spots or rafts within vesicles as well as stripes within cylindrical micelles. Calcium- and copper-crossbridged domains of synthetic block copolymers or natural lipid (phosphatidylinositol-4,5-bisphosphate) possess tunable sizes, shapes and/or spacings that can last for years. Lateral segregation in these 'ligand-responsive Janus assemblies' couples weakly to curvature and proves to be restricted within phase diagrams to narrow regimes of pH and cation concentration that are centred near the characteristic binding constants for polyacid interactions. Remixing at high pH is surprising, but a theory for strong lateral segregation shows that counterion entropy dominates electrostatic crossbridges, thus illustrating the insights gained into ligand-induced pattern formation within self-assemblies.
MeSH Terms
Cations, Divalent/chemistry
Hydrogen-Ion Concentration
Ligands
Membranes, Artificial
Micelles
Polymers/chemistry
Surface-Active Agents
Chemicals
Cations, Divalent
Ligands
Membranes, Artificial
Micelles
Polymers
Surface-Active Agents
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Christian David A
Laboratory for Research on the Structure of Matter, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Tian Aiwei
Ellenbroek Wouter G
Levental Ilya
Rajagopal Karthikan
Janmey Paul A
Liu Andrea J
Baumgart Tobias
Discher Dennis E
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