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微管成核模板机制的免疫结构证据。

Immunostructural evidence for the template mechanism of microtubule nucleation.

作者信息

Keating T J, Borisy G G

机构信息

Laboratory of Molecular Biology, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Nat Cell Biol. 2000 Jun;2(6):352-7. doi: 10.1038/35014045.

Abstract

Two opposing models have been proposed to explain how the gamma-tubulin ring complex (gammaTuRC) induces microtubule nucleation. In the 'protofilament' model, the gammaTuRC induces nucleation as a partially or completely straightened protofilament that is incorporated longitudinally into the wall of the nascent microtubule, whereas the 'template' model proposes that the gammaTuRC acts as a helical template that constitutes the base of the newly-formed polymer. Here we appraise these two models, using high-resolution structural and immunolocalization methods. We show that components of the gammaTuRC localize to a narrow zone at the extreme minus end of the microtubule and that these ends terminate in a pointed cap. Together, these results strongly favour the template model of microtubule nucleation.

摘要

为了解释γ-微管蛋白环复合物(γTuRC)如何诱导微管成核,人们提出了两种相反的模型。在“原丝”模型中,γTuRC作为部分或完全伸直的原丝诱导成核,该原丝纵向并入新生微管的壁中,而“模板”模型则提出γTuRC作为构成新形成聚合物基础的螺旋模板。在这里,我们使用高分辨率结构和免疫定位方法对这两种模型进行评估。我们表明,γTuRC的组分定位于微管极端负端的一个狭窄区域,并且这些末端终止于一个尖帽。这些结果共同强烈支持微管成核的模板模型。

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