Suppr超能文献

GDP-微管蛋白环的冷冻电子显微镜观察

Cryo-electron microscopy of GDP-tubulin rings.

作者信息

Nicholson W V, Lee M, Downing K H, Nogales E

机构信息

Lawrence Berkeley Natl. Lab. and Molecular and Cell Biology Department, UC Berkeley, CA 94720-3200, USA.

出版信息

Cell Biochem Biophys. 1999;31(2):175-83. doi: 10.1007/BF02738171.

Abstract

Rings of guanosine diphosphate (GDP)-tubulin formed in the presence of divalent cations have been studied using conventional negative stain and cryo-electron microscopy. The structure of such rings resembles that of depolymerizing microtubule ends and corresponds to an "unconstrained" conformation of tubulin in its GDP state. The use of cryo-techniques has allowed us to image the ring polymers free from dehydration and flattening artifacts. Preparations of frozen-hydrated GDP-tubulin rings are generally heterogeneous and contain a mixture of double, triple, and incomplete rings, as well as spirals and some rare single rings. Images of different polymer types can be identified and classified into groups that are then amenable for averaging and single particle reconstruction methods. Identifying the differences in tubulin structure, between straight and curve protofilaments, will be important to understand the molecular bases of dynamic instability in microtubules.

摘要

利用传统负染和冷冻电子显微镜技术,对在二价阳离子存在下形成的鸟苷二磷酸(GDP)-微管蛋白环进行了研究。这种环的结构类似于解聚的微管末端结构,对应于处于GDP状态的微管蛋白的“无约束”构象。冷冻技术的应用使我们能够对无脱水和扁平化伪影的环状聚合物进行成像。冷冻水合GDP-微管蛋白环的制备通常是异质的,包含双环、三环和不完全环的混合物,以及螺旋和一些罕见的单环。不同聚合物类型的图像可以被识别并分类成不同的组,然后适用于平均和单颗粒重建方法。识别直的和弯曲的原纤维之间微管蛋白结构的差异,对于理解微管动态不稳定性的分子基础至关重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验