4.8 Article

Electrostatic Control of Structure in Self-Assembled Membranes

Journal

SMALL
Volume 10, Issue 3, Pages 500-505

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201300254

Keywords

self-assembly; peptide amphiphiles; ordered membranes; SAXS; polyelectrolyte-supramolecular polymer complex

Funding

  1. National Institute of Biomedical Imaging and Bioengineering at the National Institutes of Health [5R01EB003806-05]
  2. NSF MRSEC program [DMR-0520513]
  3. Ben Gurion University of the Negev
  4. NSF-NSEC
  5. NSF-MRSEC
  6. Keck Foundation
  7. State of Illinois
  8. Northwestern University
  9. E.I. DuPont de Nemours Co.
  10. Dow Chemical Company
  11. U. S. DOE [DE-AC02-06CH11357]

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Self-assembling peptide amphiphiles (PAs) can form hierarchically ordered membranes when brought in contact with aqueous polyelectrolytes of the opposite charge by rapidly creating a diffusion barrier composed of filamentous nanostructures parallel to the plane of the incipient membrane. Following this event, osmotic forces and charge complexation template nanofiber growth perpendicular to the plane of the membrane in a dynamic self-assembly process. In this work, we show that this hierarchical structure requires massive interfacial aggregation of PA molecules, suggesting the importance of rapid diffusion barrier formation. Strong PA aggregation is induced here through the use of heparin-binding PAs with heparin and also with polyelectrolytes of varying charge density. Small angle X-ray scattering shows that in the case of weak PA-polyelectrolyte interaction, membranes formed display a cubic phase ordering on the nanoscale that likely results from clusters of PA nanostructures surrounded by polyelectrolyte chains.

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