Golan D E, Veatch W
Proc Natl Acad Sci U S A. 1980 May;77(5):2537-41. doi: 10.1073/pnas.77.5.2537.
Band 3, the major intrinsic protein of the human erythrocyte membrane, was specifically labeled with the covalent fluorescent probe eosin isothiocyanate. The lateral mobility of labeled band 3 in the plane of the membrane under various conditions of ionic strength and temperature was examined by using the fluorescence photobleaching recovery technique. Low temperature (21 degrees C) and high ionic strength (46 mM NaPO(4)) favored immobilization of band 3(10% mobile) as well as slow diffusion of the mobile fraction (diffusion coefficient D = 4 x 10(-11) cm(2)sec(-1)). Increasing temperature (37 degrees C) and decreasing ionic strength (13 mM NaPO(4)) led to an increase in the fraction of mobile band 3(90% mobile) and a reversible increase in the diffusion rate of the mobile fraction (D = 200 x 10(-11) cm(2)sec(-1)). The increase in the fraction of mobile band 3 was markedly dissociated, however, from the increase in the diffusion rate of the mobile fraction. Thus, the fraction of mobile band 3 always increased at higher ionic strength and lower temperature than the ionic strength and temperature at which the diffusion rate increased. This dissociation was manifested kinetically on prolonged incubation of ghosts at constant ionic strength and temperature: the diffusion rate of the mobile fraction increased slowly at first and much more rapidly after the initial lag period, whereas the fraction of mobile band 3 increased almost immediately to 90% and remained maximal for the duration of the experiment. Further, changes in diffusion rate with temperature were promptly and totally reversible, whereas increases in the mobile fraction were only slowly and partially reversible. These effects were shown not to be due to complete dissociation of spectrin, the major protein of the erythrocyte cytoskeleton, from the membrane. This evidence suggests control of band 3 lateral mobility by at least two separate processes. The process that determines the diffusion coefficient of the mobile band 3 is completely reversible, and it probably involves a metastable state of cytoskeleton structure intermediate between tight binding to the membrane and complete dissociation from it.
带3蛋白是人类红细胞膜的主要内在蛋白,用共价荧光探针异硫氰酸伊红进行特异性标记。利用荧光光漂白恢复技术,检测了在不同离子强度和温度条件下,标记的带3蛋白在膜平面内的横向流动性。低温(21℃)和高离子强度(46 mM NaPO₄)有利于带3蛋白固定化(10%可移动),以及可移动部分的缓慢扩散(扩散系数D = 4×10⁻¹¹ cm²·s⁻¹)。温度升高(37℃)和离子强度降低(13 mM NaPO₄)导致可移动带3蛋白比例增加(90%可移动),以及可移动部分扩散速率的可逆增加(D = 200×10⁻¹¹ cm²·s⁻¹)。然而,可移动带3蛋白比例的增加与可移动部分扩散速率的增加明显分离。因此,可移动带3蛋白的比例总是在比扩散速率增加时更高的离子强度和更低的温度下增加。这种分离在恒定离子强度和温度下对血影进行长时间孵育时在动力学上表现出来:可移动部分的扩散速率起初缓慢增加,在初始延迟期后增加得更快,而可移动带3蛋白的比例几乎立即增加到90%,并在实验期间保持最大值。此外,扩散速率随温度的变化迅速且完全可逆,而可移动部分的增加只是缓慢且部分可逆。这些效应并非由于红细胞细胞骨架的主要蛋白质血影蛋白与膜完全解离所致。这一证据表明,带3蛋白的横向流动性至少受两个独立过程的控制。决定可移动带3蛋白扩散系数的过程是完全可逆的,它可能涉及细胞骨架结构的亚稳态,该亚稳态介于与膜紧密结合和与膜完全解离之间。