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Related Concept Videos

Destabilization of Microtubules01:45

Destabilization of Microtubules

The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
Anaphase A and B01:39

Anaphase A and B

Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
The Contractile Ring02:15

The Contractile Ring

Contractile rings are composed of microfilaments and are responsible for separating the daughter cells during cytokinesis. Contractile ring assembly proceeds along with other cell cycle events; however, very few mechanistic details are known about the timing and coordination of the contractile rings with the cell cycle.
A small GTPase, RhoA, controls the function and assembly of the contractile ring. RhoA belongs to the Ras superfamily of proteins. The activation of formins by RhoA promotes...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
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...
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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Related Experiment Video

Updated: Jun 13, 2026

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

Force transduction by the microtubule-bound Dam1 ring.

Jonathan W Armond1, Matthew S Turner

  • 1Department of Physics, University of Warwick, Coventry, United Kingdom.

Biophysical Journal
|April 23, 2010
PubMed
Summary

Two mechanisms explain how the Dam1 ring complex stays on depolymerizing microtubules during mitosis. Novel experiments could distinguish between physical obstruction and attractive binding models for force generation.

Area of Science:

  • Cell Biology
  • Biophysics
  • Computational Biology

Background:

  • The Dam1 ring complex is crucial for force generation during mitosis, coupling microtubule depolymerization with ring motion.
  • Current understanding relies on computational models with many unconstrained parameters, hindering experimental validation.
  • Distinguishing between proposed mechanisms for Dam1 ring-microtubule interaction remains a challenge.

Purpose of the Study:

  • To identify and analyze two distinct mechanisms for Dam1 ring complex attachment to depolymerizing microtubules.
  • To propose experimental strategies for differentiating between competing models of Dam1 ring-microtubule interaction.

Main Methods:

  • Analysis of existing computational models to delineate distinct force transduction mechanisms.

More Related Videos

Directly Measuring Forces Within Reconstituted Active Microtubule Bundles
07:47

Directly Measuring Forces Within Reconstituted Active Microtubule Bundles

Published on: May 10, 2022

Analyses of Actin Dynamics, Clutch Coupling and Traction Force for Growth Cone Advance
07:53

Analyses of Actin Dynamics, Clutch Coupling and Traction Force for Growth Cone Advance

Published on: October 21, 2021

Related Experiment Videos

Last Updated: Jun 13, 2026

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

Directly Measuring Forces Within Reconstituted Active Microtubule Bundles
07:47

Directly Measuring Forces Within Reconstituted Active Microtubule Bundles

Published on: May 10, 2022

Analyses of Actin Dynamics, Clutch Coupling and Traction Force for Growth Cone Advance
07:53

Analyses of Actin Dynamics, Clutch Coupling and Traction Force for Growth Cone Advance

Published on: October 21, 2021

  • Theoretical investigation of two proposed mechanisms: physical obstruction by splayed protofilaments and attractive binding.
  • Proposal of novel experimental approaches, including altering diffusion constants and applying time-varying loads.

    • Main Results:

    • Identified two primary mechanisms: physical prevention of detachment by microtubule protofilaments and an attractive binding interaction.
    • The analysis provides a framework for experimentally distinguishing these two models.
    • Novel experimental strategies are proposed to resolve the ambiguity in current models.

    Conclusions:

    • The study clarifies two potential mechanisms for Dam1 ring complex stability on microtubules during depolymerization.
    • Proposed experimental methods offer a path to experimentally validate or refute these mechanisms.
    • Resolving these models will advance our understanding of mitotic force generation and chromosome segregation.