Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

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...
Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
Microtubules01:35

Microtubules

There are three types of cytoskeletal structures in eukaryotic cells—microfilaments, intermediate filaments, and microtubules. With a diameter of about 25 nm, microtubules are the thickest of these fibers. Microtubules carry out a variety of functions that include cell structure and support, transport of organelles, cell motility (movement), and the separation of chromosomes during cell division.Microtubules are hollow tubes whose walls are made up of globular tubulin proteins. Each tubulin...
Microtubules01:18

Microtubules

Microtubules are the thickest cytoskeletal filaments with a diameter of 25 nm. In prokaryotic organisms, microtubules are commonly found in locomotory appendages like cilia and flagella. In eukaryotic cells, microtubules form specialized extensions for moving fluid over the surface, like those found in cells lining the intestine.
Microtubules have two structurally similar globular protein subunits: α and β tubulins. In the cytosol, the α and β tubulins form a heterodimer. These αβ-heterodimers...
Additional Subnuclear Structures02:10

Additional Subnuclear Structures

The eukaryotic nucleus is a double membrane-bound organelle that contains nearly all of the cell’s genetic material in the form of chromosomes. It is rightly called the “brain” of the cell as it shoulders the responsibility of responding to various physiological processes, stress, altered metabolic conditions, and other cellular signals. 
The nucleus contains many membrane-less subnuclear organelles or nuclear bodies, such as nucleoli, Cajal bodies, speckles, paraspeckles, etc. These nuclear...
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.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Protocol to generate microglia-containing cerebral organoids to model HIV neuroinflammation.

STAR protocols·2026
Same author

MX2 Mediates Collapse of the HIV-1 Capsid.

bioRxiv : the preprint server for biology·2026
Same author

Kinesin-1 conformational dynamics are controlled by a cargo-sensitive TPR switch.

eLife·2026
Same author

Antibody escape drives emergence of diverse spike haplotypes resembling variants of concern in persistent SARS-CoV-2 infections.

Cell reports. Medicine·2026
Same author

Generation and characterization of iPSC models from HIV-1-positive individuals with divergent clinical outcomes.

Stem cell reports·2026
Same author

A murine coronavirus infection platform identifies proviral and proinflammatory activities of SARS-CoV-2 accessory protein 7a.

Journal of virology·2025

Related Experiment Video

Updated: Jul 16, 2026

Self-Assembly of Microtubule Tactoids
08:49

Self-Assembly of Microtubule Tactoids

Published on: June 23, 2022

TRIM5 alpha cytoplasmic bodies are highly dynamic structures.

Edward M Campbell1, Mark P Dodding, Melvyn W Yap

  • 1Department of Cell and Molecular Biology, Northwestern University, Chicago, IL 60611-3008, USA.

Molecular Biology of the Cell
|March 30, 2007
PubMed
Summary

Tripartite motif (TRIM)5 alpha forms dynamic cytoplasmic bodies that move along microtubules. These dynamic TRIM5 alpha bodies suggest a role in function or regulation, not static aggregation.

More Related Videos

Identification of Kinesin-1 Cargos Using Fluorescence Microscopy
08:06

Identification of Kinesin-1 Cargos Using Fluorescence Microscopy

Published on: February 14, 2016

Quantitative Microtubule Fractionation Technique to Separate Stable Microtubules, Labile Microtubules, and Free Tubulin in Mouse Tissues
07:21

Quantitative Microtubule Fractionation Technique to Separate Stable Microtubules, Labile Microtubules, and Free Tubulin in Mouse Tissues

Published on: November 17, 2023

Related Experiment Videos

Last Updated: Jul 16, 2026

Self-Assembly of Microtubule Tactoids
08:49

Self-Assembly of Microtubule Tactoids

Published on: June 23, 2022

Identification of Kinesin-1 Cargos Using Fluorescence Microscopy
08:06

Identification of Kinesin-1 Cargos Using Fluorescence Microscopy

Published on: February 14, 2016

Quantitative Microtubule Fractionation Technique to Separate Stable Microtubules, Labile Microtubules, and Free Tubulin in Mouse Tissues
07:21

Quantitative Microtubule Fractionation Technique to Separate Stable Microtubules, Labile Microtubules, and Free Tubulin in Mouse Tissues

Published on: November 17, 2023

Area of Science:

  • Virology
  • Cell Biology
  • Immunology

Background:

  • Tripartite motif (TRIM)5 alpha is a host restriction factor that inhibits retroviral infection.
  • TRIM5 alpha localizes to distinct cytoplasmic bodies, but their function is unknown.

Purpose of the Study:

  • To investigate the localization and dynamics of TRIM5 alpha cytoplasmic bodies.
  • To determine the role of these dynamic structures in TRIM5 alpha function.

Main Methods:

  • Utilized fluorescent fusion proteins and live cell microscopy.
  • Performed photobleaching and photoactivation analysis.

Main Results:

  • TRIM5 alpha cytoplasmic bodies are highly mobile, moving along microtubules.
  • Body morphology is dynamic, and TRIM5 alpha rapidly exchanges between bodies and the cytoplasm.
  • TRIM5 alpha cytoplasmic bodies are dynamic, not static aggregates.

Conclusions:

  • TRIM5 alpha cytoplasmic bodies are dynamic structures involved in TRIM5 alpha function or regulation.
  • These findings differentiate TRIM5 alpha bodies from static inclusion bodies.