Rowell C A, Kowalczyk J J, Lewis M D, Garcia A M
Eisai Research Institute, Andover, Massachusetts 01810, USA.
J Biol Chem. 1997 May 30;272(22):14093-7. doi: 10.1074/jbc.272.22.14093.
It has recently been reported that Ki-Ras protein can be modified in vitro by farnesylation or geranylgeranylation. However, a previous analysis of Ki-Ras prenylation in vivo found only farnesylated Ki-Ras. In this report it is shown that under normal conditions, Ki-Ras is farnesylated in vivo and when cells are treated with the farnesyl transferase inhibitors B956 or B957, farnesylation is inhibited and Ki-Ras becomes geranylgeranylated in a dose dependent manner. These results have strong implications in the design of anticancer drugs based on inhibition of prenylation.
最近有报道称,Ki-Ras蛋白在体外可被法尼基化或香叶基香叶基化修饰。然而,先前对体内Ki-Ras异戊二烯化的分析仅发现了法尼基化的Ki-Ras。本报告表明,在正常条件下,Ki-Ras在体内被法尼基化,当细胞用法尼基转移酶抑制剂B956或B957处理时,法尼基化受到抑制,Ki-Ras以剂量依赖的方式变成香叶基香叶基化。这些结果对基于抑制异戊二烯化的抗癌药物设计具有重要意义。