Marzouki A, Sontag B, Lavergne J P, Vidonne C, Reboud J P, Reboud A M
Laboratoire de Biochimie Médicale, Université Lyon I, CNRS, Villeurbanne, France.
Biochimie. 1991 Jul-Aug;73(7-8):1151-6. doi: 10.1016/0300-9084(91)90159-x.
Samples of unmodified EF-2, EF-2 ADP-ribosylated with diphtheria toxin and NAD, and/or phosphorylated using ATP and the Ca(2+)-calmodulin dependent kinase III partially purified, were irradiated at 254 nm with 32P-labeled GDP or GTP, and analyzed by one- and two-dimensional gel electrophoresis. By this method we showed that unmodified EF-2 formed a stable complex with GDP but not with GTP, whereas phosphorylated EF-2 and ADP-ribosylated + phosphorylated EF-2 formed stable complexes even in the absence of irradiation, with GTP but not GDP. ADP-ribosylated EF-2 did not form stable complexes with either GDP or GTP. Prior ADP-ribosylation of EF-2 increased its ability to the phosphorylated. These results show that the structures of the two domains containing diphtamide 715 and the phosphorylatable threonines (between Ala 51 and Arg 60) are interdependent; modifications of these residues induce different conformational changes of EF-2 which alter the interactions of the factor with guanylic nucleotides as well with ribosomes.
将未修饰的EF-2、用白喉毒素和NAD进行ADP-核糖基化修饰的EF-2以及/或者使用ATP和部分纯化的钙调蛋白依赖性激酶III进行磷酸化修饰的EF-2样品,用32P标记的GDP或GTP在254nm波长下进行照射,然后通过一维和二维凝胶电泳进行分析。通过这种方法我们发现,未修饰的EF-2与GDP形成稳定复合物,但不与GTP形成稳定复合物;而磷酸化的EF-2以及ADP-核糖基化+磷酸化的EF-2即使在未照射的情况下也能与GTP而非GDP形成稳定复合物。ADP-核糖基化的EF-2与GDP或GTP均不形成稳定复合物。EF-2预先进行ADP-核糖基化会增强其被磷酸化的能力。这些结果表明,含有二羟赖胺酸715和可磷酸化苏氨酸(在丙氨酸51和精氨酸60之间)的两个结构域的结构是相互依存的;这些残基的修饰会诱导EF-2发生不同的构象变化,从而改变该因子与鸟苷酸以及核糖体之间的相互作用。