Bunow M R, Levin I W
Biochim Biophys Acta. 1977 Jan 4;464(1):202-16. doi: 10.1016/0005-2736(77)90382-0.
Resonance-enhanced and normal vibrational Raman spectra were observed for both multilamellar and single-wall vesicle assemblies of dimyristoyl phosphatidylcholine containing amphotericin B, a channel-forming polyene antibiotic, and cholesterol. The decrease in the frequency of the polyene antibiotic C = C stretching mode at 1556 cm-1 and the increase in intensity of the C-C-H in-plane deformation mode at 1002 cm-1 indicate that amphotericin B is ordered in a lipid-cholesterol medium similarly to the solid, but is surrounded by a slightly more polar environment. The intensity of the C = C stretching mode I1556 decreases 4-fold during the broadened gel to liquid crystalline phase transition (16--32 degrees C) of dimyristoyl lecithin-cholesterol (4 : 1) multilayers. Other resonance-enhanced vibrations of amphotericin B exhibit similar behavior. For amphotericin B in pure dimyristoyl lecithin multilayer or vesicle systems, however, the vibrational intensity associated with the C = C stretching mode remains constant during the melting of lipid hydrocarbon chains. In addition, a third effect occurs in liquid crystalline egg lecithin-cholesterol (4 : 1, mol ratio) multilayers in which I 1556 first increases by 25% between 3 and 25 degrees C, in parallel with the loss of active channels, and then remains constant as the temperature increases from 25 to 42 degrees C. This latter intensity pattern is masked in the dimyristoyl lecithin-cholesterol system by the overwhelming effect upon the C = C mode from changes in the lipid chain packing characteristics which occur during the phase transition. The broadened phase transition in 4 : 1 dimyristoyl lecithin-cholesterol multilayers (16--32 degrees C), as followed by the ratio of intensities at 2880 and 2850 cm-1 (asymmetric and symmetric methylene C-H stretching modes, respectively) is slightly narrowed by the addition of amphotericin B, and effect from which a binding stoichiometry at 24 degrees of 1 : 1 amphotericin B: cholesterol is estimated. This stoichiometry was confirmed by differential calorimetric scans, which also show the presence of a peak proportional to cholesterol content. Raman I2880/2850 peak height ratios in pure dimyristoyl lecithin bilayers were increased over the 14--38 degrees C range by amphotericin B, a spectral effect which suggests an ordering of the lipid matrix perhaps as a consequence of the polyene binding to the bilayer surface. For bilayers containing cholesterol, the ratios of intensities of the 2935 cm-1 feature, composed mainly of acyl chain terminal methyl and underlying methylene C-H stretching modes, to the 2850 cm-1 feature are significantly increased by amphotericin B. This effect indicates that the antibiotic penetrates the bilayer in the lipid-sterol system.
观察到了含有两性霉素B(一种形成通道的多烯抗生素)和胆固醇的二肉豆蔻酰磷脂酰胆碱的多层和单壁囊泡组装体的共振增强振动拉曼光谱和正常振动拉曼光谱。在1556 cm-1处多烯抗生素C = C伸缩振动模式频率的降低以及在1002 cm-1处C-C-H面内变形振动模式强度的增加表明,两性霉素B在脂质 - 胆固醇介质中呈有序排列,类似于固体状态,但周围环境的极性稍强。在二肉豆蔻酰卵磷脂 - 胆固醇(4∶1)多层膜从宽化的凝胶相向液晶相转变(16 - 32℃)过程中,C = C伸缩振动模式的强度I1556降低了4倍。两性霉素B的其他共振增强振动也表现出类似行为。然而,对于纯二肉豆蔻酰卵磷脂多层膜或囊泡系统中的两性霉素B,与C = C伸缩振动模式相关的振动强度在脂质烃链熔化过程中保持不变。此外,在液晶态卵卵磷脂 - 胆固醇(4∶1,摩尔比)多层膜中出现了第三种效应,其中I1556在3至25℃之间首先增加25%,同时活性通道丧失,然后随着温度从25℃升高到42℃保持不变。在二肉豆蔻酰卵磷脂 - 胆固醇系统中,后一种强度模式被相变过程中脂质链堆积特征变化对C = C模式的压倒性影响所掩盖。在4∶1二肉豆蔻酰卵磷脂 - 胆固醇多层膜(16 - 32℃)中宽化的相变过程中,通过2880和2850 cm-1处强度比(分别为不对称和对称亚甲基C - H伸缩振动模式)跟踪发现,加入两性霉素B后相变略微变窄,据此估计在24℃时两性霉素B与胆固醇的结合化学计量比为1∶1。差示量热扫描证实了该化学计量比,该扫描还显示存在一个与胆固醇含量成比例的峰。在14 - 38℃范围内,两性霉素B使纯二肉豆蔻酰卵磷脂双层膜中的拉曼I2880/2850峰高比增加,这种光谱效应表明脂质基质可能由于多烯与双层表面结合而发生有序排列。对于含有胆固醇的双层膜,两性霉素B使主要由酰基链末端甲基和下层亚甲基C - H伸缩振动模式组成(2935 cm-1)的特征峰与2850 cm-1特征峰的强度比显著增加。这种效应表明抗生素在脂质 - 甾醇系统中穿透了双层膜。