Microtubule Binding

Microtubule binding is the attachment of proteins or other molecules to microtubules, dynamic polymers of α- and β-tubulin that organize the cell interior and support essential cellular functions. Binding occurs when a molecule recognizes sites on the microtubule surface or its ends; microtubule-associated proteins can stabilize or cross-link filaments, whereas kinesin and dynein use ATP hydrolysis to move cargo along them. In biology, these interactions regulate microtubule growth and shortening, chromosome segregation, cell shape, and intracellular transport. Studying microtubule binding helps explain cytoskeletal organization and supports research on motor proteins, mitosis, neurobiology, and drugs that alter microtubule dynamics.

Microtubule Binding - Related Videos

Research

JoVE EoE - Colorectal Cancer

Microtubule Binding Assay in CRC Cells: A Method to Examine Microtubule Binding Tau Protein in Colorectal Cancer Cells

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2023

This video describes the microtubule-binding assay used to separate the microtubule-binding tau protein from non-binding hyperphosphorylated tau protein fractions in colorectal cancer cells. This assay helps determine the effect of various chemicals that can alter the phosphorylation status of tau protein, affecting its microtubule binding.

Assay for Phosphorylation and Microtubule Binding Along with Localization of Tau Protein in Colorectal Cancer Cells

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Cited by 11 •

2017

This manuscript describes standard protocols for measuring tau hyperphosphorylation, measuring tau binding to microtubules, and localization of intracellular tau following drug treatments. These protocols can be used repetitively for screening drugs or other compounds that target tau hyperphosphorylation or microtubule binding.

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

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Cited by 24 •

2014

Microtubules are inherently unstable polymers, and their switching between growth and shortening is stochastic and difficult to control. Here we describe protocols using segmented microtubules with photoablatable stabilizing caps. Depolymerization of segmented microtubules can be triggered with high temporal and spatial resolution, thereby assisting analysis of motions with the disassembling microtubule ends.

Interference Reflection Microscopy for Label-Free Visualization of Microtubule Dynamics

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2025

In this video, we describe the interference reflection microscopy (IRM) technique to visualize microtubules growing on a coverslip surface in the presence of a suitable buffer. Upon illumination with incident light, the coverslip-buffer interface and buffer-microtubule interface reflect light, which combines to create an interference pattern, enabling the visualization of microtubules as high-contrast images against a bright background.

TIRF Microscopy to Visualize Actin and Microtubule Coupling Dynamics

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2025

This video describes TIRF, a total internal reflection microscopy-based technique to visualize actin and microtubule polymerization dynamics. The method allows the high-resolution imaging of actin and microtubule coupling dynamics in real-time, which is essential for understanding cellular crosstalks.

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