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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
来源:
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.
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页码:7051 / 7060
页数:10
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