Eisenberg Sharon, Henis Yoav I
Department of Neurobiochemistry, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Cell Signal. 2008 Jan;20(1):31-9. doi: 10.1016/j.cellsig.2007.07.012. Epub 2007 Aug 21.
The complex dynamic structure of the plasma membrane plays critical roles in cellular signaling; interactions with the membrane lipid milieu, spatial segregation within and between cellular membranes and/or targeting to specific membrane-associated scaffolds are intimately involved in many signal transduction pathways. In this review, we focus on the membrane interactions of Ras proteins. These small GTPases play central roles in the regulation of cell growth and proliferation, and their excessive activation is commonly encountered in human tumors. Ras proteins associate with the membrane continuously via C-terminal lipidation and additional interactions in both their inactive and active forms; this association, as well as the targeting of specific Ras isoforms to plasma membrane microdomains and to intracellular organelles, have recently been implicated in Ras signaling and oncogenic potential. We discuss biochemical and biophysical evidence for the roles of specific domains of Ras proteins in mediating their association with the plasma membrane, and consider the potential effects of lateral segregation and interactions with membrane-associated protein assemblies on the signaling outcomes.
质膜复杂的动态结构在细胞信号传导中起着关键作用;与膜脂环境的相互作用、细胞膜内及细胞膜间的空间分隔和/或靶向特定的膜相关支架,都密切参与了许多信号转导途径。在本综述中,我们聚焦于Ras蛋白的膜相互作用。这些小GTP酶在细胞生长和增殖的调控中发挥核心作用,其过度激活在人类肿瘤中普遍存在。Ras蛋白在其非活性和活性形式下均通过C末端脂化及其他相互作用持续与膜结合;这种结合,以及特定Ras亚型靶向质膜微结构域和细胞内细胞器,最近被认为与Ras信号传导和致癌潜能有关。我们讨论了Ras蛋白特定结构域在介导其与质膜结合中作用的生化和生物物理证据,并考虑了侧向分隔以及与膜相关蛋白组装体的相互作用对信号转导结果的潜在影响。