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相关概念视频

Microtubule Formation01:23

Microtubule Formation

Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation of...
Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
Microtubule Instability02:17

Microtubule Instability

Microtubules are hollow cylindrical filaments having a diameter of approximately 25 nm and a length that varies from 200 nm to 25 μm. GTP-bound tubulin subunits form αβ-heterodimers for microtubule assembly. These core building blocks interact longitudinally, polymerizing into protofilaments. The protofilaments then interact with one another through lateral bonding forces to form stable cylindrical microtubules. These cylindrical filaments are dynamic as they undergo repeated assembly and...
Microtubule Instability02:17

Microtubule Instability

Microtubules are hollow cylindrical filaments having a diameter of approximately 25 nm and a length that varies from 200 nm to 25 μm. GTP-bound tubulin subunits form αβ-heterodimers for microtubule assembly. These core building blocks interact longitudinally, polymerizing into protofilaments. The protofilaments then interact with one another through lateral bonding forces to form stable cylindrical microtubules. These cylindrical filaments are dynamic as they undergo repeated assembly and...
Coat Assembly and GTPases01:33

Coat Assembly and GTPases

Vesicles incorporate different coat protein subunits in different cell locations, which changes the properties of the coat, such as the shape and geometry of the transport vesicles. Thus, vesicle coat proteins also play a significant role in cargo selection.
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
Microtubule Associated Proteins (MAPs)01:42

Microtubule Associated Proteins (MAPs)

Microtubule function and architecture are regulated by an array of specialized proteins called microtubule-associated proteins or MAPs. These proteins are widespread across different organisms and have conserved protein motifs, like the multi-TOG domain for tubulin binding found in the CLASP family of MAPs. Some MAPs are lineage-specific based on their conserved domains. Their functions depend upon the cytoskeletal architecture and cell type they are located within. In-plant cells, a specific...

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相关实验视频

Updated: May 23, 2026

Extracting Modified Microtubules from Mammalian Cells to Study Microtubule-Protein Complexes by Cryo-Electron Microscopy
08:02

Extracting Modified Microtubules from Mammalian Cells to Study Microtubule-Protein Complexes by Cryo-Electron Microscopy

Published on: March 3, 2023

在成长中的微管末端,EBs识别出核酸依赖的结构盖.

Sebastian P Maurer1, Franck J Fourniol, Gergő Bohner

  • 1Cancer Research UK London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.

Cell
|April 17, 2012
PubMed
概括

末结合蛋白 (EBs) 通过结合特定结构来跟踪生长的微管末端. 这项研究揭示了Mal3 EB是如何形成的.

科学领域:

  • 细胞生物学 细胞生物学
  • 结构生物学 结构生物学
  • 生物化学 生物化学

背景情况:

  • 微管子生长的末端是调节微管子动态的蛋白质的关键结合点.
  • 末端结合蛋白 (EBs) 识别并结合这些动态微管末端,招募其他因素.
  • 对于EB识别生长的微管末端的精确结构基础在很大程度上是未知的.

研究的目的:

  • 确定裂变酵母EB Mal3的calponin同质 (CH) 域如何与生长中的微管末结合的伪原子模型.
  • 阐明EBs.认可的微管末端区域的结构特征.
  • 了解微管末端结构,EB结合和微管动力学之间的关系.

主要方法:

  • 低温电子显微镜 (cryo-EM) 用于高分辨率的结构确定.
  • 亚纳米单粒子重建以构建伪原子模型.
  • 光成像用于验证 in situ 的结合和动态.

主要成果:

  • 产生了 Mal3 CH 域与生长中的微管末结合的伪原子模型.
  • 观察到Mal3 CH域跨越了微管原细丝,不包括.
  • 结合发生在GTP结合部位附近,这表明对核酸状态的敏感性.

更多相关视频

Preparation of Segmented Microtubules to Study Motions Driven by the Disassembling Microtubule Ends
12:20

Preparation of Segmented Microtubules to Study Motions Driven by the Disassembling Microtubule Ends

Published on: March 15, 2014

Using plusTipTracker Software to Measure Microtubule Dynamics in Xenopus laevis Growth Cones
07:32

Using plusTipTracker Software to Measure Microtubule Dynamics in Xenopus laevis Growth Cones

Published on: September 7, 2014

相关实验视频

Last Updated: May 23, 2026

Extracting Modified Microtubules from Mammalian Cells to Study Microtubule-Protein Complexes by Cryo-Electron Microscopy
08:02

Extracting Modified Microtubules from Mammalian Cells to Study Microtubule-Protein Complexes by Cryo-Electron Microscopy

Published on: March 3, 2023

Preparation of Segmented Microtubules to Study Motions Driven by the Disassembling Microtubule Ends
12:20

Preparation of Segmented Microtubules to Study Motions Driven by the Disassembling Microtubule Ends

Published on: March 15, 2014

Using plusTipTracker Software to Measure Microtubule Dynamics in Xenopus laevis Growth Cones
07:32

Using plusTipTracker Software to Measure Microtubule Dynamics in Xenopus laevis Growth Cones

Published on: September 7, 2014

结论:

  • 该结构揭示了EB如何识别和结合动态微管末端.
  • 结合EB与微管细胞的核酸结合部位有空间联系,有可能感知其状态.
  • 这提供了微管的动态不稳定性和EBs的终端追踪机制之间的结构联系.