Zakharova O M, Rosenkranz A A, Sobolev A S
Department of Biomembranes, Russian Research Center of Molecular Diagnostics and Therapy, Moscow, Russian Federation.
Biochim Biophys Acta. 1995 May 24;1236(1):177-84. doi: 10.1016/0005-2736(95)00047-7.
The technique of fluorescence recovery after photobleaching was used to measure the lateral mobility of membrane integral proteins in reticulocyte plasma membranes which were treated to modify the 'fluid' lipid or immobilized protein fractions, hence increasing the relative prevalence of obstacles to protein lateral motion. This was achieved by either: (1) treating the plasma membranes with phospholipase A2 followed by extraction of the hydrolysis products using fatty-acid-free bovine serum albumin, resulting in a decrease in the membrane 'fluid' lipid portion; or (2) preincubating the plasma membranes with polylysines, resulting in plasma membrane protein aggregation and immobilization. As the prevalence of obstacles to lateral motion increased in plasma membranes through the treatments described above, the mobility of the membrane integral proteins diminished. Experimental results for the dependence of protein mobility on the prevalence of obstacles to lateral motion were compared to theoretical data in order to verify the applicability of the percolation theory to reticulocyte plasma membranes. The influence of a decrease in the 'fluid' lipid and an increase in the immobilized membrane protein fractions upon the hormone-stimulated adenylate cyclase activity has been studied as well. As the 'solid' lipid and immobilized membrane protein fractions decreased, both the hormone-stimulated adenylate cyclase activity and the fraction of beta-adrenergic receptors with high affinity to hormone diminished. It was shown that this correlation can be caused by a decrease in membrane fraction accessible to the movement of the interacting proteins of the adenylate cyclase complex. Hormonal stimulation of adenylate cyclase is discussed in terms of the percolation theory.
采用光漂白后荧光恢复技术来测量网织红细胞质膜中膜整合蛋白的侧向流动性,这些质膜经过处理以改变“流体”脂质或固定化蛋白组分,从而增加蛋白侧向运动障碍的相对发生率。这通过以下两种方式实现:(1)用磷脂酶A2处理质膜,然后用无脂肪酸的牛血清白蛋白提取水解产物,导致膜“流体”脂质部分减少;或(2)将质膜与聚赖氨酸预孵育,导致质膜蛋白聚集和固定化。随着通过上述处理质膜中侧向运动障碍的发生率增加,膜整合蛋白的流动性降低。将蛋白流动性对侧向运动障碍发生率的依赖性实验结果与理论数据进行比较,以验证渗流理论对网织红细胞质膜的适用性。还研究了“流体”脂质减少和固定化膜蛋白组分增加对激素刺激的腺苷酸环化酶活性的影响。随着“固体”脂质和固定化膜蛋白组分减少,激素刺激的腺苷酸环化酶活性以及对激素具有高亲和力的β-肾上腺素能受体组分均降低。结果表明,这种相关性可能是由于腺苷酸环化酶复合物相互作用蛋白运动可及的膜组分减少所致。从渗流理论的角度讨论了腺苷酸环化酶的激素刺激作用。