Chen James M, Friedman Fred K, Brandt-Rauf Paul W, Pincus Matthew R, Chie Lyndon
Structural Chemistry, Gilead Sciences, Foster City, CA 94404, USA.
J Protein Chem. 2002 Jul;21(5):349-59. doi: 10.1023/a:1019994302273.
GTPase activating protein (GAP) is a known regulator of ras-p21 activity and is a likely target of ras-induced mitogenic signaling. The domains of GAP that may be involved in this signaling are unknown. In order to infer which domains of GAP may be involved, we have performed molecular dynamics calculations of GAP complexed to wild-type and oncogenic (Val 12-containing) ras-p21, both bound to GTP. We have computed and superimposed the average structures for both complexes and find that there are four domains of GAP that undergo major changes in conformation: residues 821-851, 917-924, 943-953, and 1003-1020. With the exception of the 943-953 domain, none of these domains is involved in making contacts with ras-p21, and all of them occur on the surface of the protein, making them good candidates for effector domains. In addition, three ras-p21 domains undergo major structural changes in the oncogenic p21-GAP complex: 71-76 from the switch 2 domain; 100-108, which interacts with SOS, jun and jun kinase (JNK); and residues 122-138. The change in conformation of the 71-76 domain appears to be induced by changes in conformation in the switch 1 domain (residues 32-40) and in the adjacent domain involving residues 21-31. In an accompanying paper, we present results from microinjection of peptides corresponding to each of these domains into oocytes induced to undergo maturation by oncogenic ras-p21 and by insulin-activated wild-type cellular p21 to determine whether these domain peptides may be involved in ras signaling through GAP.
GTP酶激活蛋白(GAP)是已知的ras - p21活性调节剂,可能是ras诱导的有丝分裂信号转导的靶点。GAP中可能参与该信号转导的结构域尚不清楚。为了推断GAP的哪些结构域可能参与其中,我们对与野生型和致癌性(含Val 12)的ras - p21(均结合GTP)形成复合物的GAP进行了分子动力学计算。我们计算并叠加了两种复合物的平均结构,发现GAP有四个结构域的构象发生了重大变化:821 - 851位残基、917 - 924位残基、943 - 953位残基和1003 - 1020位残基。除了943 - 953结构域外,这些结构域均不参与与ras - p21的接触,并且它们都出现在蛋白质表面,使其成为效应结构域很好的候选者。此外,在致癌性p21 - GAP复合物中,三个ras - p21结构域发生了重大结构变化:来自开关2结构域的71 - 76位残基;与SOS、jun和jun激酶(JNK)相互作用的100 - 108位残基;以及122 - 138位残基。71 - 76结构域构象的变化似乎是由开关1结构域(32 - 40位残基)和涉及21 - 31位残基的相邻结构域的构象变化诱导的。在一篇配套论文中,我们展示了将与这些结构域中的每一个对应的肽显微注射到由致癌性ras - p21和胰岛素激活的野生型细胞p21诱导成熟的卵母细胞中的结果,以确定这些结构域肽是否可能通过GAP参与ras信号转导。