Rimon G, Meyerstein N, Henis Y I
Biochim Biophys Acta. 1984 Sep 5;775(3):283-90. doi: 10.1016/0005-2736(84)90182-2.
The lateral diffusion coefficients (D) and the mobile fractions of the fluorescent phospholipid N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)phosphatidylethanolamine (NBD-PE) and of membrane proteins labelled with fluorescein isothiocyanate, were measured by fluorescence photobleaching recovery on erythrocytes from healthy persons and from a hereditary spherocytosis patient. Measurements of lipid probe mobility were performed on ghosts labelled by NBD-PE exclusively at the external monolayer, or at both sides of the membrane. Our results indicate the following: (1) The mean values and the temperature dependence of D are different at the external and internal membrane leaflets. (2) In both normal and HS ghosts the mobile fraction of NBD-PE in the external monolayer does not depend significantly on temperature. On the other hand, the mobile fraction in the internal monolayer is reduced as the temperature is decreased. (3) At low temperatures, the mobile fraction of NBD-PE in the internal monolayer of spherocytic ghosts is significantly lower than the mobile fraction in the internal monolayer of normal ghosts. (4) No differences were observed between the mobilities of membrane proteins in normal and in spherocytic ghosts. However, differences were observed between the two cell populations in the temperature-dependence of the intrinsic fluorescence of unlabelled membrane proteins. The implications of these results for membrane phospholipid asymmetry and for cytoskeletal interactions with the internal lipid monolayer are discussed.
通过荧光漂白恢复技术,测量了健康人和遗传性球形红细胞增多症患者红细胞中荧光磷脂N-(7-硝基苯并-2-恶唑-1,3-二氮杂环丁烷-4-基)磷脂酰乙醇胺(NBD-PE)以及异硫氰酸荧光素标记的膜蛋白的横向扩散系数(D)和移动分数。脂质探针流动性的测量仅在仅由NBD-PE标记于外部单层或膜两侧的血影上进行。我们的结果表明:(1)膜外部和内部小叶的D的平均值和温度依赖性不同。(2)在正常和HS血影中,外部单层中NBD-PE的移动分数对温度的依赖性不显著。另一方面,内部单层中的移动分数随着温度降低而降低。(3)在低温下,球形红细胞血影内部单层中NBD-PE的移动分数显著低于正常血影内部单层中的移动分数。(4)正常血影和球形红细胞血影中膜蛋白的流动性未观察到差异。然而,在两个细胞群体中,未标记膜蛋白的固有荧光的温度依赖性存在差异。讨论了这些结果对膜磷脂不对称性以及细胞骨架与内部脂质单层相互作用的意义。