Choy E, Chiu V K, Silletti J, Feoktistov M, Morimoto T, Michaelson D, Ivanov I E, Philips M R
Department of Medicine, New York University School of Medicine, New York 10016, USA.
Cell. 1999 Jul 9;98(1):69-80. doi: 10.1016/S0092-8674(00)80607-8.
We show that Nras is transiently localized in the Golgi prior to the plasma membrane (PM). Moreover, green fluorescent protein (GFP)-tagged Nras illuminated motile, peri-Golgi vesicles, and prolonged BFA treatment blocked PM expression. GFP-Hras colocalized with GFP-Nras, but GFP-Kras4B revealed less Golgi and no vesicular fluorescence. Whereas a secondary membrane targeting signal was required for PM expression, the CAAX motif alone was necessary and sufficient to target proteins to the endomembrane where they were methylated, a modification required for efficient membrane association. Thus, prenylated CAAX proteins do not associate directly with the PM but instead associate with the endomembrane and are subsequently transported to the PM, a process that requires a secondary targeting motif.
我们发现,Nras在定位于质膜(PM)之前会短暂地定位于高尔基体。此外,绿色荧光蛋白(GFP)标记的Nras照亮了动态的高尔基体周围小泡,延长的BFA处理会阻断质膜表达。GFP-Hras与GFP-Nras共定位,但GFP-Kras4B显示出较少的高尔基体且无小泡荧光。虽然质膜表达需要第二个膜靶向信号,但单独的CAAX基序对于将蛋白质靶向内膜是必要且充分的,在内膜中它们会被甲基化,这是有效膜结合所需的修饰。因此,异戊二烯化的CAAX蛋白不会直接与质膜结合,而是与内膜结合,随后被转运到质膜,这一过程需要第二个靶向基序。