Department of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, Oregon, USA.
Biophys J. 2013 Feb 5;104(3):594-603. doi: 10.1016/j.bpj.2012.12.041.
The hydrophobic surfactant proteins, SP-B and SP-C, greatly accelerate the adsorption of the surfactant lipids to an air/water interface. Previous studies of factors that affect curvature suggest that vesicles may adsorb via a rate-limiting structure with prominent negative curvature, in which the hydrophilic face of the lipid leaflets is concave. To determine if SP-B and SP-C might promote adsorption by inducing negative curvature, we used small-angle x-ray scattering to test whether the physiological mixture of the two proteins affects the radius of cylindrical monolayers in the inverse hexagonal phase. With dioleoyl phosphatidylethanolamine alone, the proteins had no effect on the hexagonal lattice constant, suggesting that the proteins fail to insert into the cylindrical monolayers. The surfactant lipids also contain ∼10% anionic phospholipids, which might allow incorporation of the cationic proteins. With 10% of the anionic dioleoyl phosphatidylglycerol added to dioleoyl phosphatidylethanolamine, the proteins induced a dose-related decrease in the hexagonal lattice constant. At 30°C, the reduction reached a maximum of 8% relative to the lipids alone at ∼1% (w/w) protein. Variation of NaCl concentration tested whether the effect of the protein represented a strictly electrostatic effect that screening by electrolyte would eliminate. With concentrations up to 3 M NaCl, the dose-related change in the hexagonal lattice constant decreased but persisted. Measurements at different hydrations determined the location of the pivotal plane and proved that the change in the lattice constant produced by the proteins resulted from a shift in spontaneous curvature. These results provide the most direct evidence yet that the surfactant proteins can induce negative curvature in lipid leaflets. This finding supports the model in which the proteins promote adsorption by facilitating the formation of a negatively curved, rate-limiting structure.
疏水性表面活性剂蛋白 SP-B 和 SP-C 极大地促进了表面活性剂脂质向气/水界面的吸附。先前对影响曲率的因素的研究表明,囊泡可能通过具有显著负曲率的限速结构吸附,其中脂质双层的亲水面是凹面的。为了确定 SP-B 和 SP-C 是否可以通过诱导负曲率来促进吸附,我们使用小角度 X 射线散射来测试这两种蛋白质的生理混合物是否会影响反六方相中的圆柱形单层的半径。单独使用二油酰基磷脂酰乙醇胺时,蛋白质对六方晶格常数没有影响,这表明蛋白质不能插入圆柱形单层中。表面活性剂脂质还含有约 10%的阴离子磷脂,这可能允许阳离子蛋白质的掺入。在添加 10%的阴离子二油酰基磷脂酰甘油后,蛋白质诱导了与剂量相关的六方晶格常数的降低。在 30°C 时,与单独的脂质相比,在约 1%(w/w)蛋白质时,减少了相对最大 8%。NaCl 浓度的变化测试了蛋白质的作用是否代表一种严格的静电效应,电解质的屏蔽作用可以消除这种效应。在高达 3 M 的 NaCl 浓度下,与剂量相关的六方晶格常数的变化减小但仍然存在。在不同水合作用下的测量确定了关键平面的位置,并证明了蛋白质引起的晶格常数的变化是由于自发曲率的变化。这些结果提供了迄今为止最直接的证据,证明表面活性剂蛋白可以在脂质双层中诱导负曲率。这一发现支持了这样的模型,即蛋白质通过促进形成负曲率的限速结构来促进吸附。