Cooperstein S J, Watkins D T
Department of Anatomy, University of Connecticut Health Center, Farmington 06030, USA.
Biochem Biophys Res Commun. 1995 Oct 4;215(1):75-81. doi: 10.1006/bbrc.1995.2435.
In our studies on the control of fusion of secretion granules with the plasma membrane which occurs during exocytosis, we have recently found that Ca++ and calmodulin stimulated the fusion of isolated parotid secretion granules with isolated inside-out plasma membrane vesicles. We are now examining the possibility that they do so by stimulating protein phosphorylation. Secretion granules were isolated from rat parotid by differential and gradient centrifugation and incubated with [Y32P]ATP. The granules were solubilized with sodium dodecylsulfate and the proteins resolved on a 7-15% polyacrylamide gel. Calmodulin plus Ca++, but neither alone, stimulated phosphorylation of four proteins with molecular masses of 64, 58, 55 and 31 kDa, and decreased the phosphorylation of a 36 kDa protein. Trifluoperazine and calmidazolium inhibited these effects. The results suggest that Ca++ and calmodulin may facilitate fusion of secretion granules with the plasma membrane by changing the phosphorylation state of one or more secretion granule proteins.
在我们关于胞吐作用过程中分泌颗粒与质膜融合控制的研究中,我们最近发现钙离子(Ca++)和钙调蛋白能刺激分离的腮腺分泌颗粒与分离的内翻质膜囊泡的融合。我们现在正在研究它们是否通过刺激蛋白质磷酸化来实现这一作用。通过差速离心和梯度离心从大鼠腮腺中分离出分泌颗粒,并与[γ32P]ATP一起孵育。用十二烷基硫酸钠使颗粒溶解,蛋白质在7 - 15%的聚丙烯酰胺凝胶上进行分离。钙调蛋白加钙离子(Ca++)能刺激分子量为64、58、55和31 kDa的四种蛋白质的磷酸化,且单独使用两者均无此作用,同时降低了一种36 kDa蛋白质的磷酸化。三氟拉嗪和氯米帕明抑制了这些作用。结果表明,钙离子(Ca++)和钙调蛋白可能通过改变一种或多种分泌颗粒蛋白的磷酸化状态来促进分泌颗粒与质膜的融合。