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首页> 外文期刊>Chembiochem: A European journal of chemical biology >Differential Effects of Natural Product Microtubule Stabilizers on Microtubule Assembly: Single Agent and Combination Studies with Taxol, Epothilone B, and Discodermolide
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Differential Effects of Natural Product Microtubule Stabilizers on Microtubule Assembly: Single Agent and Combination Studies with Taxol, Epothilone B, and Discodermolide

机译:天然产物微管稳定剂对微管组装的差异作用:与紫杉醇,埃坡霉素B和Discodermolide的单药和组合研究

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摘要

A systematic comparison has been performed of the morphology and stability of microtubules (MTs) induced by the potent microtubule-stabilizing agents (MSAs) taxol, epothilone B (Epo B), and discodermolide (DDM) under GTP-free conditions. DDM-induced tubulin polymerization occurred significantly faster than that induced by taxol and Epo B. At the some time, tubulin polymers assembled from soluble tubulin by DDM were morphologically distinct (shorter and less ordered) from those induced by either taxol or Epo B, as demonstrated by electron microscopy. Exposure of MSA-induced tubulin polymers to ultrasound revealed the DDM-based polymers to be less stable to this type of physical stress than those formed with either Epo B or taxol. Interestingly, PAT assembly in the presence of both DDM and taxol appeared to produce a distinct new type of PAT polymer with a mixed morphology between those of DDM- and taxol-induced structures. The observed differences in MT morphology and stability might be related, at least partly, to differences in intramicrotubular tubulin isotype distribution, as DDM showed a different pattern of beta-tubulin isotype usage in the assembly process.
机译:在无GTP的条件下,对由有效的微管稳定剂(MSA)紫杉醇,埃坡霉素B(Epo B)和Discodermolide(DDM)诱导的微管(MTs)的形态和稳定性进行了系统的比较。 DDM诱导的微管蛋白聚合反应比紫杉醇和Epo B诱导的微管蛋白聚合发生的速度显着加快。在一段时间内,DDM从可溶性微管蛋白组装的微管蛋白聚合物在形态学上与紫杉醇或Epo B诱导的微管蛋白在形态上截然不同(更短,次序更少),例如由电子显微镜证实。 MSA诱导的微管蛋白聚合物在超声中的暴露表明,与用Epo B或紫杉醇形成的聚合物相比,基于DDM的聚合物对这种类型的物理应力不那么稳定。有趣的是,在DDM和紫杉醇同时存在的情况下,PAT组装似乎产生了一种独特的新型PAT聚合物,在DDM和紫杉醇诱导的结构之间混合了形态。观察到的MT形态和稳定性差异可能至少部分与微管内微管蛋白同种型分布的差异有关,因为DDM在组装过程中显示出不同的β-微管蛋白同种型使用模式。

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