Stenger Patrick C, Alonso Coralie, Zasadzinski Joseph A, Waring Alan J, Jung Chun-Ling, Pinkerton Kent E
Department of Chemical Engineering, University of California, Santa Barbara, CA 93106-5080, USA.
Biochim Biophys Acta. 2009 Feb;1788(2):358-70. doi: 10.1016/j.bbamem.2008.11.021. Epub 2008 Dec 11.
Adsorption of the clinical lung surfactants (LS) Curosurf or Survanta from aqueous suspension to the air-water interface progresses from multi-bilayer aggregates through multilayer films to a coexistence between multilayer and monolayer domains. Exposure to environmental tobacco smoke (ETS) alters this progression as shown by Langmuir isotherms, fluorescence microscopy and atomic force microscopy (AFM). After 12 h of LS exposure to ETS, AFM images of Langmuir-Blodgett deposited films show that ETS reduces the amount of material near the interface and alters how surfactant is removed from the interface during compression. For Curosurf, ETS prevents refining of the film composition during cycling; this leads to higher minimum surface tensions. ETS also changes the morphology of the Curosurf film by reducing the size of condensed phase domains from 8-12 microm to approximately 2 microm, suggesting a decrease in the line tension between the domains. The minimum surface tension and morphology of the Survanta film are less impacted by ETS exposure, although the amount of material associated with the film is reduced in a similar way to Curosurf. Fluorescence and mass spectra of Survanta dispersions containing native bovine SP-B treated with ETS indicate the oxidative degradation of protein aromatic amino acid residue side chains. Native bovine SP-C isolated from ETS exposed Survanta had changes in molecular mass consistent with deacylation of the lipoprotein. Fourier Transform Infrared Spectroscopy (FTIR) characterization of the hydrophobic proteins from ETS treated Survanta dispersions show significant changes in the conformation of SP-B and SP-C that correlate with the altered surface activity and morphology of the lipid-protein film.
临床肺表面活性剂(LS)珂立苏或固尔苏从水悬浮液吸附到气-水界面的过程,是从多层聚集体经过多层膜发展到多层域和单层域共存。如朗缪尔等温线、荧光显微镜和原子力显微镜(AFM)所示,暴露于环境烟草烟雾(ETS)会改变这一过程。在LS暴露于ETS 12小时后,朗缪尔-布洛杰特沉积膜的AFM图像显示,ETS减少了界面附近的物质数量,并改变了压缩过程中表面活性剂从界面去除的方式。对于珂立苏,ETS会阻止循环过程中膜成分的细化;这会导致更高的最低表面张力。ETS还通过将凝聚相域的尺寸从8-12微米减小到约2微米来改变珂立苏膜的形态,这表明域之间的线张力降低。尽管与膜相关的物质数量与珂立苏以类似方式减少,但固尔苏膜的最低表面张力和形态受ETS暴露的影响较小。含有经ETS处理的天然牛SP-B的固尔苏分散体的荧光和质谱表明蛋白质芳香族氨基酸残基侧链发生了氧化降解。从暴露于ETS的固尔苏中分离出的天然牛SP-C的分子量发生了变化,这与脂蛋白的脱酰作用一致。对经ETS处理的固尔苏分散体中的疏水蛋白进行傅里叶变换红外光谱(FTIR)表征,结果显示SP-B和SP-C的构象发生了显著变化,这与脂蛋白膜的表面活性和形态改变相关。