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具有可切换机械性能的肽膜的界面结构和杨氏模量。

The interfacial structure and Young's modulus of peptide films having switchable mechanical properties.

作者信息

Middelberg A P J, He L, Dexter A F, Shen H-H, Holt S A, Thomas R K

机构信息

Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, Queensland 4072, Australia.

出版信息

J R Soc Interface. 2008 Jan 6;5(18):47-54. doi: 10.1098/rsif.2007.1063.

Abstract

We report the structure and Young's modulus of switchable films formed by peptide self-assembly at the air-water interface. Peptide surfactant AM1 forms an interfacial film that can be switched, reversibly, from a high- to low-elasticity state, with rapid loss of emulsion and foam stability. Using neutron reflectometry, we find that the AM1 film comprises a thin (approx. 15A) layer of ordered peptide in both states, confirming that it is possible to drastically alter the mechanical properties of an interfacial ensemble without significantly altering its concentration or macromolecular organization. We also report the first experimentally determined Young's modulus of a peptide film self-assembled at the air-water interface (E=80MPa for AM1, switching to E<20MPa). These findings suggest a fundamental link between E and the macroscopic stability of peptide-containing foam. Finally, we report studies of a designed peptide surfactant, Lac21E, which we find forms a stronger switchable film than AM1 (E=335MPa switching to E<4MPa). In contrast to AM1, Lac21E switching is caused by peptide dissociation from the interface (i.e. by self-disassembly). This research confirms that small changes in molecular design can lead to similar macroscopic behaviour via surprisingly different mechanisms.

摘要

我们报道了在空气-水界面通过肽自组装形成的可切换薄膜的结构和杨氏模量。肽表面活性剂AM1形成一种界面薄膜,它可以从高弹性状态可逆地切换到低弹性状态,同时乳液和泡沫稳定性迅速丧失。利用中子反射技术,我们发现AM1薄膜在两种状态下均包含一层薄的(约15埃)有序肽层,这证实了在不显著改变其浓度或大分子组织的情况下,有可能大幅改变界面体系的机械性能。我们还报道了首个通过实验测定的在空气-水界面自组装的肽膜的杨氏模量(AM1的E = 80MPa,切换后E < 20MPa)。这些发现表明E与含肽泡沫的宏观稳定性之间存在根本联系。最后,我们报道了对一种设计的肽表面活性剂Lac21E的研究,我们发现它形成的可切换薄膜比AM1更强(E = 335MPa切换后E < 4MPa)。与AM1不同,Lac21E的切换是由肽从界面解离(即通过自组装)引起的。这项研究证实,分子设计上的微小变化可以通过惊人的不同机制导致相似的宏观行为。

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