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A unified model for microtubule rescue

机译:统一的微管抢救模型

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How microtubules transition from depolymerization to polymerization, known as rescue, is poorly understood. Here we examine two models for rescue: 1) an “end-driven” model in which the depolymerizing end stochastically switches to a stable state; and 2) a “lattice-driven” model in which rescue sites are integrated into the microtubule before depolymerization. We test these models using a combination of computational simulations and in vitro experiments with purified tubulin. Our findings support the “lattice-driven” model by identifying repeated rescue sites in microtubules. In addition, we discover an important role for divalent cations in determining the frequency and location of rescue sites. We use “wash-in” experiments to show that divalent cations inhibit rescue during depolymerization, but not during polymerization. We propose a unified model in which rescues are driven by embedded rescue sites in microtubules, but the activity of these sites is influenced by changes in the depolymerizing ends.
机译:微管如何从解聚转变为聚合(称为拯救),人们对此知之甚少。在这里,我们研究了两种用于救援的模型:1)“端驱动”模型,其中解聚端随机切换到稳定状态; 2)“晶格驱动”模型,其中在解聚之前将救援位点整合到微管中。我们使用计算仿真和纯化微管蛋白的体外实验相结合的方法测试这些模型。我们的发现通过识别微管中的重复营救位点来支持“晶格驱动”模型。此外,我们发现二价阳离子在确定营救地点的频率和位置方面起着重要作用。我们使用“冲洗”实验表明二价阳离子在解聚过程中抑制了拯救,但在聚合过程中却没有。我们提出了一个统一的模型,在该模型中,救援是由微管中嵌入的救援位点驱动的,但是这些位点的活动受解聚末端变化的影响。

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