Lateral phase separation in interfacial films of pulmonary surfactant

被引:102
作者
Discher, BM
Maloney, KM
Schief, WR
Grainger, DW
Vogel, V
Hall, SB
机构
[1] OREGON HLTH SCI UNIV, DEPT BIOCHEM, PORTLAND, OR 97201 USA
[2] OREGON HLTH SCI UNIV, DEPT MED, PORTLAND, OR 97201 USA
[3] OREGON GRAD INST SCI & TECHNOL, DEPT CHEM BIOCHEM & MOL BIOL, PORTLAND, OR 97006 USA
[4] UNIV WASHINGTON, CTR BIOENGN, SEATTLE, WA 98195 USA
[5] COLORADO STATE UNIV, DEPT CHEM, FT COLLINS, CO 80523 USA
关键词
D O I
10.1016/S0006-3495(96)79450-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To determine if lateral phase separation occurs in films of pulmonary surfactant, we used epifluorescence microscopy and Brewster angle microscopy (BAM) to study spread films of calf lung surfactant extract (CLSE). Both microscopic methods demonstrated that compression produced domains of liquid-condensed lipids surrounded by a liquid-expanded film, The temperature dependence of the pressure at which domains first emerged for CLSE paralleled the behavior of its most prevalent component, dipalmitoyl phosphatidylcholine (DPPC), although the domains appeared at pressures 8-10 mN/m higher than for DPPC over the range of 20-37 degrees C. The total area occupied by the domains at room temperature increased to a maximum value at 35 mN/m during compression. The area of domains reached 25 +/- 5% of the interface, which corresponds to the predicted area of DPPC in the monolayer, At pressures above 35 mN/m, however, both epifluorescence and BAM showed that the area of the domains decreased dramatically. These studies therefore demonstrate a pressure-dependent gap in the miscibility of surfactant constituents. The monolayers separate into two phases during compression but remain largely miscible at higher and lower surface pressures.
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页码:2583 / 2590
页数:8
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