Koyama S, Williams L T, Kikuchi A
Department of Biochemistry, Hiroshima University School of Medicine, Japan.
FEBS Lett. 1995 Jul 17;368(2):321-5. doi: 10.1016/0014-5793(95)00686-4.
Several deletion mutants of Raf-1 were expressed with v-ras p21 or 14-3-3 protein in COS-7 cells and Sf9 cells and the interaction of Raf-1 with ras p21 or with 14-3-3 protein in intact cells was examined. Raf(1-135) (residues 1-135) and Raf(1-322) interacted with v-ras p21, but other deletion mutants such as Raf(136-322) or Raf(321-648) did not. Raf(1-322) interacted with 14-3-3 protein much more efficiently than Raf(321-648) did. While Raf(1-135) did not interact with 14-3-3 protein, Raf(136-322) did. These results clearly indicate that Raf-1 simultaneously interacts with both ras p21 and 14-3-3 protein through the distinct binding domains in intact cells.
在COS-7细胞和Sf9细胞中,用v-ras p21或14-3-3蛋白表达了几种Raf-1缺失突变体,并检测了完整细胞中Raf-1与ras p21或14-3-3蛋白的相互作用。Raf(1-135)(第1至135位氨基酸残基)和Raf(1-322)与v-ras p21相互作用,但其他缺失突变体如Raf(136-322)或Raf(321-648)则不与v-ras p21相互作用。Raf(1-322)与14-3-3蛋白的相互作用比Raf(321-648)更有效。虽然Raf(1-135)不与14-3-3蛋白相互作用,但Raf(136-322)则与之相互作用。这些结果清楚地表明,在完整细胞中,Raf-1通过不同的结合结构域同时与ras p21和14-3-3蛋白相互作用。