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首页> 外文期刊>Biochemistry >Purification and characterization of assembly-competent tubulin from Aspergillus nidulans.
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Purification and characterization of assembly-competent tubulin from Aspergillus nidulans.

机译:构巢曲霉中具有装配能力的微管蛋白的纯化和鉴定。

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摘要

We have developed a procedure for purifying assembly-competent tubulin from Aspergillus nidulans. To our knowledge, this is the first report of the purification of assembly-competent tubulin from a filamentous fungus, and the procedure should be of great value in analyzing the large number of alpha- and beta-tubulin mutations that have been isolated and characterized in A. nidulans. Our procedure consists of overproduction of alpha- and beta-tubulin, partial purification by ion-exchange chromatography, and final purification by rounds of assembly and disassembly. We have found that taxol promotes the assembly of A. nidulans tubulin into microtubules, but a higher concentration of taxol is required for maximal assembly of A. nidulans tubulin than is required for brain tubulin. The critical concentration for assembly in the presence of taxol is also significantly higher for A. nidulans tubulin than for brain tubulin. In addition, A. nidulans microtubules that were assembled and maintained in the presenceof taxol depolymerized in conditions in which taxol-stabilized mammalian microtubules remain intact. These results suggest that A. nidulans tubulin has a lower affinity for taxol than mammalian tubulin.
机译:我们已经开发了一种从构巢曲霉中纯化具有装配能力的微管蛋白的程序。据我们所知,这是从丝状真菌中纯化具有装配能力的微管蛋白的第一份报告,该方法在分析已分离和鉴定的大量α-和β-微管蛋白突变中应具有重要价值。 A. nidulans。我们的程序包括过量生产α-和β-微管蛋白,通过离子交换色谱法部分纯化以及通过几轮组装和拆卸的最终纯化。我们发现紫杉醇促进构巢曲霉微管蛋白组装成微管,但是最大组装数的构巢曲霉微管蛋白需要比脑微管蛋白更高的紫杉醇浓度。对于构巢曲霉微管蛋白,在紫杉醇存在下组装的临界浓度也显着高于脑微管蛋白。另外,在紫杉醇存在下组装和维持的构巢曲霉微管在紫杉醇稳定的哺乳动物微管保持完整的条件下解聚。这些结果表明,构巢曲霉微管蛋白对紫杉醇的亲和力比哺乳动物微管蛋白低。

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