Arnal I, Wade R H
Laboratoire de Microscopie Electronique Structurale, Institute de Biologie Structurale Jean-Pierre Ebel (CEA, CNRS), Grenoble, France.
Curr Biol. 1995 Aug 1;5(8):900-8. doi: 10.1016/s0960-9822(95)00180-1.
The antimitotic agent taxol is an important new drug for the treatment of certain cancers. It blocks the cell cycle in its G1 or M phases by stabilizing the microtubule cytoskeleton against depolymerization.
We have used electron cryomicroscopy and image analysis to investigate the structure of microtubules assembled in vitro, and found that their fine structure was sensitive to the presence of taxol. The conformation of the microtubule lattice depended on whether the drug was added before or after assembly. The structure of preassembled microtubules changed only slightly when taxol was added; a larger change was observed when microtubules were assembled in the presence of the drug. In both cases, taxol-containing microtubules were stable over many days at, or below, room temperature.
As in another recent investigation using guanylyl-(alpha,beta)-methylene-diphosphonate (a non-hydrolyzable GTP analogue), microtubule stabilization with taxol is accompanied by a conformational change in the microtubule surface lattice and, implicitly, in the tubulin dimer. We speculate that a general mechanism may underlie the stabilization of microtubules by different agents.
抗有丝分裂药物紫杉醇是治疗某些癌症的一种重要新药。它通过稳定微管细胞骨架防止解聚,从而阻断细胞周期的G1期或M期。
我们利用电子低温显微镜和图像分析技术研究了体外组装的微管结构,发现其精细结构对紫杉醇的存在很敏感。微管晶格的构象取决于药物是在组装前还是组装后添加。添加紫杉醇时,预组装微管的结构仅略有变化;在药物存在的情况下组装微管时,观察到更大的变化。在这两种情况下,含紫杉醇的微管在室温或室温以下可稳定存在许多天。
正如最近另一项使用鸟苷酰 -(α,β)-亚甲基二磷酸酯(一种不可水解的GTP类似物)的研究所表明的那样,紫杉醇使微管稳定的同时,微管表面晶格以及隐含的微管蛋白二聚体也会发生构象变化。我们推测,不同药物使微管稳定可能存在一个共同的机制。