Reversible active switching of the mechanical properties of a peptide film at a fluid-fluid interface

被引:127
作者
Dexter, Annette F. [1 ]
Malcolm, Andrew S. [1 ]
Middelberg, Anton P. J. [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Ctr Biomol Engn, St Lucia, Qld 4072, Australia
关键词
D O I
10.1038/nmat1653
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Designer peptides have recently been developed as building blocks for novel self-assembled materials with stimuli-responsive properties. To date, such materials have been based on self-assembly in bulk aqueous solution or at solid-fluid interfaces. We have designed a 21-residue peptide, AM1, as a stimuli-responsive surfactant that switches molecular architectures at a fluid-fluid interface in response to changes in bulk aqueous solution composition. In the presence of divalent zinc at neutral pH, the peptide forms a mechanically strong 'film state'. In the absence of metal ions or at acid pH, the peptide adsorbs to form a mobile 'detergent state'. The two interfacial states can be actively and reversibly switched. Switching between the two states by a change in pH or the addition of a chelating agent leads to rapid emulsion coalescence or foam collapse. This work introduces a new class of surfactants that offer an environmentally friendly approach to control the stability of interfaces in foams, emulsions and fluid-fluid interfaces more generally.
引用
收藏
页码:502 / 506
页数:5
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