Adsorbed layers of ferritin at solid and fluid interfaces studied by atomic force microscopy

被引:57
作者
Johnson, CA [1 ]
Yuan, Y [1 ]
Lenhoff, AM [1 ]
机构
[1] Univ Delaware, Dept Chem Engn, Ctr Mol & Engn Thermodynam, Newark, DE 19716 USA
基金
美国国家航空航天局;
关键词
proteins; scanning probe microscopy; electrostatic double-layer interactions; random sequential adsorption;
D O I
10.1006/jcis.1999.6680
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
The adsorption of the iron storage protein ferritin was studied by liquid tapping mode atomic force microscopy in order to obtain molecular resolution in the adsorbed layer within the aqueous environment in which the adsorption was carried out. The surface coverage and the structure of the adsorbed layer were investigated as functions of ionic strength and pH on two different charged surfaces, namely chemically modified glass slides and mixed surfactant films at the air-water interface, which were transferred to graphite substrates after adsorption. Surface coverage trends with both ionic strength and pH indicate the dominance of electrostatic effects, with the balance shifting between intermolecular repulsion and protein-surface attraction. The resulting behavior is more complex than that seen for larger colloidal particles, which appear to follow a modified random sequential adsorption model monotonically. The structure of the adsorbed layers at the solid surfaces is random, but some indication of long-range order is apparent at fluid interfaces, presumably due to the higher protein mobility at the fluid interface. (C) 2000 Academic Press.
引用
收藏
页码:261 / 272
页数:12
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