Linear and nonlinear microrheology of lysozyme layers forming at the air-water interface

被引:26
|
作者
Allan, Daniel B. [1 ]
Firester, Daniel M. [1 ]
Allard, Victor P. [1 ]
Reich, Daniel H. [1 ]
Stebe, Kathleen J. [2 ]
Leheny, Robert L. [1 ]
机构
[1] Johns Hopkins Univ, Dept Phys & Astron, Baltimore, MD 21218 USA
[2] Univ Penn, Dept Biomol & Chem Engn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
STRUCTURAL CONFORMATION; RHEOLOGICAL PROPERTIES; ACTIVE MICRORHEOLOGY; AIR/WATER INTERFACE; BROWNIAN DYNAMICS; SURFACE RHEOLOGY; PROTEIN; DRAG; VISCOELASTICITY; DENATURATION;
D O I
10.1039/c4sm00484a
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
We report experiments studying the mechanical evolution of layers of the protein lysozyme adsorbing at the air-water interface using passive and active microrheology techniques to investigate the linear and nonlinear rheological response, respectively. Following formation of a new interface, the linear shear rheology, which we interrogate through the Brownian motion of spherical colloids at the interface, becomes viscoelastic with a complex modulus that has approximately power-law frequency dependence. The power-law exponent characterizing this frequency dependence decreases steadily with increasing layer age. Meanwhile, the nonlinear microrheology, probed via the rotational motion of magnetic nanowires at the interface, reveals a layer response characteristic of a shear-thinning power-law fluid with a flow index that decreases with age. We discuss two possible frameworks for understanding this mechanical evolution: gelation and the formation of a soft glass phase.
引用
收藏
页码:7051 / 7060
页数:10
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