Wang H G, Rapp U R, Reed J C
The Burnham Institute, Program on Apoptosis and Cell Death Research, La Jolla, California 92037, USA.
Cell. 1996 Nov 15;87(4):629-38. doi: 10.1016/s0092-8674(00)81383-5.
A green fluorescent protein (GFP)-Raf-1 fusion protein was used to show that Bcl-2 can target this kinase to mitochondria. Active Raf-1 fused with targeting sequences from an outer mitochondrial membrane protein protected cells from apoptosis and resulted in phosphorylation of BAD, a proapoptotic Bcl-2 homolog. Plasma membrane-targeted Raf-1 did not protect from apoptosis and resulted in phosphorylation of ERK-1 and ERK-2. Untargeted active Raf-1 improved Bcl-2-mediated resistance to apoptosis, whereas a kinase-inactive Raf-1 mutant abrogated apoptosis suppression by Bcl-2. Bcl-2 can therefore target Raf-1 to mitochondrial membranes, allowing this kinase to phosphorylate BAD or possibly other protein substrates involved in apoptosis regulation.
绿色荧光蛋白(GFP)-Raf-1融合蛋白被用于证明Bcl-2可将这种激酶靶向至线粒体。与线粒体外膜蛋白的靶向序列融合的活性Raf-1保护细胞免于凋亡,并导致促凋亡Bcl-2同源物BAD的磷酸化。靶向质膜的Raf-1不能保护细胞免于凋亡,并导致ERK-1和ERK-2的磷酸化。未靶向的活性Raf-1增强了Bcl-2介导的抗凋亡能力,而激酶失活的Raf-1突变体则消除了Bcl-2对凋亡的抑制作用。因此,Bcl-2可将Raf-1靶向至线粒体膜,使这种激酶能够磷酸化BAD或可能参与凋亡调节的其他蛋白质底物。