Chen S Y, Cheng K H
Physics Department, Texas Tech University, Lubbock 79409.
Chem Phys Lipids. 1990 Dec;56(2-3):149-58. doi: 10.1016/0009-3084(90)90097-b.
Fourier transform infrared (FTIR) and time-resolved fluorescence spectroscopy have been employed to examine the structural dynamics of lipid fatty acyl chains and lipid/water interfacial region of a binary lipid mixture containing unsaturated phosphatidylethanolamine (PE) and diacylglycerol (DG). Infrared vibrational frequencies of the CH2 symmetric stretching and the C = O stretching bands of the lipids were measured at different lipid compositions and temperatures. For 0% DG, the lamellar gel to lamellar liquid crystalline (L beta-L alpha) and the L alpha to inverted hexagonal (L alpha-HII) phase transitions were observed at approximately 15 degrees and 55 degrees C, respectively. As the DG content increased gradually from 0% to 15%, the L alpha-HII phase transition temperature decreased drastically while the L beta-L alpha phase transition temperature decreased only slightly. At 10% DG, a merge of these two phase transitions was noticed at approximately 10 degrees C. For the composition study at 23 degrees C, the L alpha-HII transition occurred at approximately 6-10% DG as indicated by abrupt increases in both the CH2 and C = O stretching frequencies at those DG contents. Using time-resolved fluorescence spectroscopy, abrupt decreases in both the normalized long time residual and the initial slope of the anisotropy decay function of lipid probes, 1-palmitoyl-2-[[2-[4-(6-phenyl-trans-1,3,5- hexatrienyl)phenyl]ethyl]carbonyl]-3-sn-phosphatidylcholine, in these PE/DG mixtures were observed at the L alpha-HII phase transition. These changes in the anisotropy decay parameters suggested that the rotational dynamics and orientational packing of the lipids were altered at the composition-induced L alpha-HII transition, and agreed with a previous temperature-induced L alpha-HII transition study on pure unsaturated PE (Cheng (1989) Biophys. J. 55, 1025-1031). The fluorescence lifetime of water soluble probes, 8,1-anilinonapthalenes sulfonate acid, in PE/DG mixtures increased abruptly at the L alpha-HII phase transition, suggesting that the conformation and hydration of the lipid/water interfacial region also undergo significant changes at the L alpha-HII transition.
傅里叶变换红外光谱(FTIR)和时间分辨荧光光谱已被用于研究含有不饱和磷脂酰乙醇胺(PE)和二酰基甘油(DG)的二元脂质混合物中脂质脂肪酰链的结构动力学以及脂质/水界面区域。在不同的脂质组成和温度下测量了脂质的CH2对称伸缩振动和C = O伸缩振动带的红外振动频率。对于0% DG,在约15℃和55℃分别观察到层状凝胶到层状液晶(Lβ-Lα)以及Lα到反相六角形(Lα-HII)的相变。随着DG含量从0%逐渐增加到15%,Lα-HII相变温度急剧下降,而Lβ-Lα相变温度仅略有下降。在10% DG时,在约10℃注意到这两个相变合并。对于23℃的组成研究,如在那些DG含量下CH2和C = O伸缩频率的突然增加所示,Lα-HII转变发生在约6 - 10% DG。使用时间分辨荧光光谱,在这些PE/DG混合物的Lα-HII相变处观察到脂质探针1-棕榈酰-2-[[2-[4-(6-苯基反式-1,3,5-己三烯基)phenyl]乙基]羰基]-3-sn-磷脂酰胆碱的归一化长时间残余和各向异性衰减函数的初始斜率均突然下降。各向异性衰减参数的这些变化表明,在组成诱导的Lα-HII转变时脂质的旋转动力学和取向堆积发生了改变,这与先前对纯不饱和PE的温度诱导的Lα-HII转变研究一致(Cheng(1989)Biophys. J. 55, 1025 - 1031)。水溶性探针8,1-苯胺基萘磺酸在PE/DG混合物中的荧光寿命在Lα-HII相变处突然增加,表明脂质/水界面区域的构象和水合作用在Lα-HII转变时也发生了显著变化。