Florine-Casteel K
Curriculum in Toxicology, University of North Carolina, Chapel Hill 27599.
Biophys J. 1990 Jun;57(6):1199-215. doi: 10.1016/S0006-3495(90)82639-4.
Low-light digitized video fluorescence microscopy has been utilized to measure the steady-state polarized fluorescence from the membrane probe diphenylhexatriene (DPH) and its cationic and phosphatidylcholine derivatives 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene (TMA-DPH) and 2-[3-(diphenylhexatrienyl)propanoyl]-3-palmitoyl-L-alpha-phosphati dylcholine (DPH-PC), respectively, in cell-size (10-70 microns) unilamellar vesicles composed of gel-or fluid-phase phospholipid. Using an inverted microscope with epi-illumination optics and an intensified silicon intensified target camera interfaced to a minicomputer, fluorescence images of single vesicles were obtained at emission polarizer orientations of 0 degrees, 45 degrees, 90 degrees, and 135 degrees relative to the excitation light polarization direction. Fluorescence intensity ratios F90 degrees/F0 degrees (= F perpendicular/F parallel) and F135 degrees/F45 degrees were calculated on a pixel-by-pixel basis from digitized image pairs. Theoretical expressions were derived for collected polarized fluorescence as a function of position on the membrane surface as well as the degree of lipid order, in terms of the fluorophore's maximum angular motional freedom in the bilayer (identical to theta max), using a modification of the method of D. Axelrod (1979. Biophys. J. 26:557-574) together with the "wobbling-in-a-cone" model of probe rotational diffusion. Comparison of experimental polarization ratios with theoretical ratios yielded the following results. In gel-phase dipalmitoyl-phosphatidylcholine, the data for all three probes correspond to a model in which the cone angle theta max = 17 +/- 2 degrees and there exists a collective tilt of the phospholipid acyl chains of 30 degrees relative to the bilayer normal. In addition, approximately 5% of DPH and TMA-DPH molecules are aligned parallel to the plane of the bilayer. In fluid-phase palmitoyloleoyl-phosphatidylcholine, the data are well fit by models in which theta max = 60 +/- 2 degrees for DPH and DPH-PC and 32 +/- 4 degrees for TMA-DPH, with approximately 20% of DPH molecules and 10% of TMA-DPH molecules aligned parallel to the bilayer plane, and a net phospholipid tilt at or near the headgroup region of approximately 30 degrees. The results demonstrate that lipid order can be measured with a spatial resolution of approximately 1 micron2 in cell-size vesicles even with high aperture observation through a microscope.
低光数字化视频荧光显微镜已被用于测量膜探针二苯基己三烯(DPH)及其阳离子和磷脂酰胆碱衍生物1-(4-三甲基铵苯基)-6-苯基-1,3,5-己三烯(TMA-DPH)和2-[3-(二苯基己三烯基)丙酰基]-3-棕榈酰-L-α-磷脂酰胆碱(DPH-PC)在由凝胶相或液相磷脂组成的细胞大小(10-70微米)单层囊泡中的稳态偏振荧光。使用配备落射照明光学系统的倒置显微镜和与小型计算机相连的增强型硅增强靶相机,在相对于激发光偏振方向为0度、45度、90度和135度的发射偏振器方向上获取单个囊泡的荧光图像。从数字化图像对逐像素计算荧光强度比F90度/F0度(=F垂直/F平行)和F135度/F45度。利用D.阿克塞尔罗德(1979年。《生物物理杂志》26:557-574)方法的改进以及探针旋转扩散的“锥内摆动”模型,推导了收集到的偏振荧光作为膜表面位置以及脂质有序度函数的理论表达式,该表达式基于荧光团在双层中的最大角运动自由度(等同于θmax)。实验偏振比与理论比的比较得出以下结果。在凝胶相二棕榈酰磷脂酰胆碱中,所有三种探针的数据都符合一个模型,其中锥角θmax = 17±2度,磷脂酰基链相对于双层法线存在30度的集体倾斜。此外,约5%的DPH和TMA-DPH分子与双层平面平行排列。在液相棕榈酰油酰磷脂酰胆碱中,数据与以下模型拟合良好:DPH和DPH-PC的θmax = 60±2度,TMA-DPH的θmax = 32±4度,约20%的DPH分子和10%的TMA-DPH分子与双层平面平行排列,并且在头部基团区域或其附近存在约30度的净磷脂倾斜。结果表明,即使通过显微镜进行高孔径观察,也可以在细胞大小的囊泡中以约1微米²的空间分辨率测量脂质有序度。