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On the Nature and Shape of Tubulin Trails: Implications on Microtubule Self-Organization

机译:微管蛋白小径的性质和形状:对微管自组织的影响。

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Microtubules, major elements of the cell skeleton are, most of the time, well organized in vivo, but they can also show self-organizing behaviors in time and/or space in purified solutions in vitro. Theoretical studies and models based on the concepts of collective dynamics in complex systems, reaction–diffusion processes and emergent phenomena were proposed to explain some of these behaviors. In the particular case of microtubule spatial self-organization, it has been advanced that microtubules could behave like ants, self-organizing by ‘talking to each other’ by way of hypothetic (because never observed) concentrated chemical trails of tubulin that are expected to be released by their disassembling ends. Deterministic models based on this idea yielded indeed like-looking spatio-temporal self-organizing behaviors. Nevertheless the question remains of whether microscopic tubulin trails produced by individual or bundles of several microtubules are intense enough to allow microtubule self-organization at a macroscopic level. In the present work, by simulating the diffusion of tubulin in microtubule solutions at the microscopic scale, we measure the shape and intensity of tubulin trails and discuss about the assumption of microtubule self-organization due to the production of chemical trails by disassembling microtubules. We show that the tubulin trails produced by individual microtubules or small microtubule arrays are very weak and not elongated even at very high reactive rates. Although the variations of concentration due to such trails are not significant compared to natural fluctuations of the concentration of tubuline in the chemical environment, the study shows that heterogeneities of biochemical composition can form due to microtubule disassembly. They could become significant when produced by numerous microtubule ends located in the same place. Their possible formation could play a role in certain conditions of reaction. In particular, it gives a mesoscopic basis to explain the collective dynamics observed in excitable microtubule solutions showing the propagation of concentration waves of microtubules at the millimeter scale, although we doubt that individual microtubules or bundles can behave like molecular ants.
机译:微管是细胞骨架的主要元素,在大多数情况下,它们在体内组织良好,但它们也可以在体外纯化溶液中显示出时间和/或空间的自组织行为。提出了基于复杂系统中集体动力学,反应扩散过程和涌现现象的理论研究和模型来解释其中的某些行为。在微管空间自组织的特殊情况下,已经提出微管可以像蚂蚁一样行为,通过假设(因为从未观察到)“预计彼此相互作用”的微管蛋白集中化学痕迹“彼此交谈”而自组织。因其拆卸目的而被释放。基于这种想法的确定性模型确实产生了时空相似的时空自组织行为。然而,仍然存在这样的问题,即由单个或成束的几个微管产生的微观微管蛋白轨迹是否足够强烈以至于在宏观水平上允许微管自组织。在目前的工作中,通过在微观尺度上模拟微管蛋白在微管溶液中的扩散,我们测量了微管蛋白轨迹的形状和强度,并讨论了由于分解微管而产生化学轨迹而引起的微管自组织的假设。我们表明,由单个微管或小的微管阵列产生的微管蛋白轨迹非常弱,即使在很高的反应速率下也不会伸长。尽管与化学环境中微管素浓度的自然波动相比,由这种痕迹引起的浓度变化并不显着,但研究表明,由于微管分解,会形成生化成分的异质性。当由位于同一位置的大量微管末端产生时,它们可能变得很重要。它们的可能形成可能在某些反应条件下起作用。尤其是,它提供了介观的基础来解释在可激发的微管溶液中观察到的集体动力学,该动力学显示了毫米级的微管浓度波的传播,尽管我们怀疑单个微管或束的行为可能像分子蚂蚁。

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  • 来源
    《Acta Biotheoretica》 |2012年第2期|p.55-82|共28页
  • 作者

    Nicolas Glade;

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