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γ-微管蛋白环复合物:解析主要脊椎动物微管核形成蛋白的分子组织和组装机制。

The gamma-tubulin ring complex: Deciphering the molecular organization and assembly mechanism of a major vertebrate microtubule nucleator.

机构信息

Zentrum für Molekulare Biologie der Universität Heidelberg, Heidelberg, Germany.

出版信息

Bioessays. 2021 Aug;43(8):e2100114. doi: 10.1002/bies.202100114. Epub 2021 Jun 23.

Abstract

Microtubules are protein cylinders with functions in cell motility, signal sensing, cell organization, intracellular transport, and chromosome segregation. One of the key properties of microtubules is their dynamic architecture, allowing them to grow and shrink in length by adding or removing copies of their basic subunit, the heterodimer αβ-tubulin. In higher eukaryotes, de novo assembly of microtubules from αβ-tubulin is initiated by a 2 MDa multi-subunit complex, the gamma-tubulin ring complex (γ-TuRC). For many years, the structure of the γ-TuRC and the function of its subunits remained enigmatic, although structural data from the much simpler yeast counterpart, the γ-tubulin small complex (γ-TuSC), were available. Two recent breakthroughs in the field, high-resolution structural analysis and recombinant reconstitution of the complex, have revolutionized our knowledge about the architecture and function of the γ-TuRC and will form the basis for addressing outstanding questions about biogenesis and regulation of this essential microtubule organizer.

摘要

微管是一种蛋白质圆柱体,在细胞运动、信号感应、细胞组织、细胞内运输和染色体分离等方面具有重要功能。微管的一个关键特性是其动态结构,允许它们通过添加或去除其基本亚基αβ-微管蛋白的副本来增长和缩短。在高等真核生物中,从头组装微管由一个 2MDa 的多亚基复合物γ-微管蛋白环复合物(γ-TuRC)启动。多年来,γ-TuRC 的结构及其亚基的功能仍然是一个谜,尽管来自结构简单得多的酵母对应物γ-微管蛋白小复合物(γ-TuSC)的结构数据是可用的。该领域的两个最新突破,即该复合物的高分辨率结构分析和重组重建,彻底改变了我们对γ-TuRC 的结构和功能的认识,并将为解决关于该基本微管组织因子的生物发生和调控的悬而未决的问题提供基础。

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