Electrostatic Control of Structure in Self-Assembled Membranes

被引:34
作者
Bitton, Ronit [1 ]
Chow, Lesley W. [2 ]
Zha, R. Helen [2 ]
Velichko, Yuri S. [2 ]
Pashuck, E. Thomas [2 ]
Stupp, Samuel I. [1 ,2 ,3 ,4 ]
机构
[1] Northwestern Univ, Inst BioNanotechnol Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
self-assembly; peptide amphiphiles; ordered membranes; SAXS; polyelectrolyte-supramolecular polymer complex; POLYELECTROLYTE-SURFACTANT COMPLEXES; NATURAL POLYELECTROLYTE; PEPTIDE AMPHIPHILES; NANOSTRUCTURES; NANOPARTICLE; TRANSITION; NANOFIBERS; MOLECULES; CRYSTALS;
D O I
10.1002/smll.201300254
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:500 / 505
页数:6
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