Macdonald T L, Humphreys W G, Martin R B
Science. 1987 Apr 10;236(4798):183-6. doi: 10.1126/science.3105058.
It has been proposed that aluminum ion is a contributing factor in a variety of neurological diseases. In many of these diseases, aberrations in the cytoskeleton have been noted. The effects of aluminum ion on the in vitro assembly of tubulin into microtubules has been examined by determining the association constants for the metal ion-guanosine triphosphate-tubulin ternary complex required for polymerization. The association constant for aluminum ion was approximately 10(7) times that of magnesium ion, the physiological mediator of microtubule assembly. In addition, aluminum ion at 4.0 X 10(-10) mole per liter competed effectively with magnesium ion for support of tubulin polymerization when magnesium ion falls below 1.0 millimole per liter. The microtubules produced by aluminum ion were indistinguishable from those produced by magnesium ion when viewed by electron microscopy, and they showed identical critical tubulin concentrations for assembly and sensitivities to cold-induced depolymerization. However, the rate of guanosine triphosphate hydrolysis and the sensitivity to calcium ion-induced depolymerization, critical regulatory processes of microtubules in vivo, were markedly lower for aluminum ion microtubules than for magnesium ion microtubules.
有人提出铝离子是多种神经疾病的一个促成因素。在许多这类疾病中,已注意到细胞骨架存在异常。通过测定聚合所需的金属离子 - 三磷酸鸟苷 - 微管蛋白三元复合物的缔合常数,研究了铝离子对微管蛋白在体外组装成微管的影响。铝离子的缔合常数约为镁离子(微管组装的生理介质)的缔合常数的10^7倍。此外,当镁离子浓度低于1.0毫摩尔/升时,每升4.0×10^(-10)摩尔的铝离子能有效地与镁离子竞争,以支持微管蛋白聚合。用电镜观察时,铝离子产生的微管与镁离子产生的微管无法区分,并且它们在组装时显示出相同的临界微管蛋白浓度以及对冷诱导解聚的敏感性。然而,对于铝离子微管,三磷酸鸟苷水解速率以及对钙离子诱导解聚的敏感性(微管在体内的关键调节过程)明显低于镁离子微管。