Suda T, Maeda N, Shiga T
J Biochem. 1980 Jun;87(6):1703-13. doi: 10.1093/oxfordjournals.jbchem.a132914.
The effect of cholesterol on the membrane fluidity of human erythrocytes has been studied by electron spin resonance (ESR) spectroscopy, sensing the motion of androstane and fatty acid spin labeles in the cell membrane and in vesicles made from extracted phospholipids. 1. Androstane spin label (ASL) was incorporated from ASL-containing phospholipid vesicles into the erythrocyte membrane, essentially by a partition mechanism in proportion to their phospholipid contents. 2. On increasing the cholesterol or ASl content in the cell membrane, the spin label was gradually immobilized. 3. ASL motion in the cell membrane seemed to be primarily determined by the cholesterol/phospholipid molar ratio, regardless of the membrane protein-lipid interaction, as judged from the temperature effects on the ESR spectra of both membranes. 4. However, glutaraldehyde pretreatment induced considerable changes of the cholesterol-lipid interaction in the cell membrane, i.e., strong immobilization and cluster formation of ASL were observed.
通过电子自旋共振(ESR)光谱研究了胆固醇对人红细胞膜流动性的影响,该光谱可检测细胞膜以及由提取的磷脂制成的囊泡中雄甾烷和脂肪酸自旋标记物的运动。1. 雄甾烷自旋标记物(ASL)基本上通过与磷脂含量成比例的分配机制,从含ASL的磷脂囊泡掺入红细胞膜。2. 增加细胞膜中的胆固醇或ASL含量时,自旋标记物逐渐固定化。3. 根据温度对两种膜的ESR光谱的影响判断,细胞膜中ASL的运动似乎主要由胆固醇/磷脂摩尔比决定,而与膜蛋白 - 脂质相互作用无关。4. 然而,戊二醛预处理引起细胞膜中胆固醇 - 脂质相互作用的显著变化,即观察到ASL的强烈固定化和聚集形成。