Feigin A M, Schagina L V, Takemoto J Y, Teeter J H, Brand J G
Monell Chemical Senses Center, Philadelphia, PA 19104-3308, USA.
Biochim Biophys Acta. 1997 Feb 21;1324(1):102-10. doi: 10.1016/s0005-2736(96)00214-3.
The ability of three sterols of different structure to influence the interaction of syringomycin E (an antifungal antibiotic that forms voltage dependent channels in planar lipid bilayers) with a planar lipid bilayer was evaluated. The rate of increase of bilayer conductance induced by syringomycin E was about 1000-times less in bilayers containing 50 mol% of cholesterol compared to bilayers without sterols. The effect of ergosterol (the primary sterol of fungal cells) on the sensitivity of bilayers to syringomycin E was much weaker than that of cholesterol, while stigmasterol (one of the main sterols of plant cells) did not significantly influence the ability of syringomycin E to induce a conductance increase in the bilayer. None of the sterols altered the single channel conductance properties of syringomycin E. These observations suggest that cholesterol affects the sensitivity of target membranes to syringomycin E by enlarging the energy barrier for channel formation rather than participating in channel formation itself.
评估了三种不同结构的甾醇影响丁香霉素E(一种在平面脂质双分子层中形成电压依赖性通道的抗真菌抗生素)与平面脂质双分子层相互作用的能力。与不含甾醇的双分子层相比,含有50摩尔%胆固醇的双分子层中,丁香霉素E诱导的双分子层电导增加速率约低1000倍。麦角固醇(真菌细胞的主要甾醇)对双分子层对丁香霉素E敏感性的影响远弱于胆固醇,而豆甾醇(植物细胞的主要甾醇之一)对丁香霉素E诱导双分子层电导增加的能力没有显著影响。这些甾醇均未改变丁香霉素E的单通道电导特性。这些观察结果表明,胆固醇通过扩大通道形成的能量屏障而非自身参与通道形成来影响靶膜对丁香霉素E的敏感性。