Structure of SP-B/DPPC Mixed Films Studied by Neutron Reflectometry

被引:6
|
作者
Fullagar, W. K. [1 ]
Holt, S. A. [2 ]
Gentle, I. R. [1 ]
机构
[1] Univ Queensland, Sch Mol & Microbial Sci, Brisbane, Qld 4072, Australia
[2] Rutherford Appleton Lab, ISIS, Pulsed Neutron & Muon Source, Didcot OX11 0QX, Oxon, England
关键词
D O I
10.1529/biophysj.108.134395
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The structures of films of pulmonary surfactant protein B (SP-B) and mixtures of SP-B and dipalmitoylphosphatidylcholine (DPPC) at the air/water interface have been studied by neutron reflectometry and Langmuir film balance methods. From the film balance studies, we observe that the isotherms of pure DPPC and SP-B/DPPC mixtures very nearly overlay one another at very high pressures, suggesting that the SP-B is being excluded from the film. The use of multiple contrasts with neutron reflectometry at a range of surface pressures has enabled the mixing and squeeze out of the DPPC and SP-B mixtures to be studied. We can identify the SP-B component of the interfacial structure and its position as a function of surface pressure. The mixtures are initially a homogeneous layer at low surface pressures. At higher surface pressures, the SP-B is squeezed out of the lipid layer into the subphase, with the first signs detected at 30 mN m(-1). At 50mN m(-1), the subphase is almost completely excluded from the DPPC layer, with the SP-B content significantly reduced. Only a small amount of DPPC appears to be associated with the squeezed out SP-B.
引用
收藏
页码:4829 / 4836
页数:8
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