Osei A A, Everett G W, Himes R H
Department of Biochemistry, University of Kansas, Lawrence 66045.
FEBS Lett. 1990 Dec 10;276(1-2):85-7. doi: 10.1016/0014-5793(90)80513-i.
In an attempt to determine whether the tightly bound Mg2+ found in purified tubulin in associated with the N-site GTP or the E-site GDP or GTP, we removed the E-site nucleotide by several means: (i) alkaline phosphatase treatment; (ii) displacement using excess GMPPCP; and (iii) polymerizing tubulin in the presence of alkaline phosphatase and non-hydrolyzable analogues. The Mg2+ content remained equal to about 1 mol/mol tubulin under conditions where denaturation did not occur. Moreover, the Mg/GTP ratio always remained equal to 1. These results indicate that the Mg2+ is associated with the N-site GTP.
为了确定在纯化微管蛋白中紧密结合的Mg2+是与N位点的GTP还是E位点的GDP或GTP相关联,我们通过几种方法去除了E位点核苷酸:(i)碱性磷酸酶处理;(ii)用过量的GMPPCP置换;以及(iii)在碱性磷酸酶和不可水解类似物存在的情况下使微管蛋白聚合。在未发生变性的条件下,Mg2+含量保持约为每摩尔微管蛋白1摩尔。此外,Mg/GTP比率始终保持为1。这些结果表明Mg2+与N位点的GTP相关联。