Self-assembly behavior of a rod-like polypeptide at the air-water interface

被引:6
|
作者
Reiter, Renate [1 ,2 ]
Wintzenrieth, Frederic [1 ]
Reiter, Guenter [1 ,2 ]
机构
[1] Univ Freiburg, Expt Polymer Phys, Hermann Herder Str 3, D-79104 Freiburg, Germany
[2] Freiburg Ctr Interact Mat & Bioinspired Technol F, D-79110 Freiburg, Germany
关键词
Polypeptide monolayer; Helical rods; Coalescence of fibers; BENZYL-L-GLUTAMATE; LIQUID-CRYSTALS; MONOLAYERS; POLY(GAMMA-BENZYL-L-GLUTAMATE); DYNAMICS; SYSTEM; PEPTIDES; FILMS;
D O I
10.1016/j.polymer.2016.08.023
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We present a systematic study of morphological changes in monolayers of a rod-like polypeptide (poly-gamma-benzyl-L-glutamate (PBLG)) on a Langmuir trough as a function of increasing surface density. Through the combination of atomic force and Brewster angle microscopy, we accessed structural information on the nano-and micro-scale. Already during the spreading process, aggregates formed, leading to a coexistence of randomly organized domains, consisting of preferentially oriented fibers, embedded in a less ordered matrix of lower density. The resulting morphology after spreading resembles a structure of a 2D foam as observed for small amphiphilic molecules. With increasing surface density, we observed that the domains became larger with fibers showing a strong tendency to coarsen. Due to this coarsening process, the plateau region of the surface pressure isotherm exhibited a continuous increase in width of the fibers. In the region of highest surface density, solid-like films composed of compacted wide fibers were observed. These fibers, which were most likely in a glassy state, were fully oriented orthogonal to the compression direction. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:379 / 386
页数:8
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