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

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Mechanism of Ciliary Motion01:05

Mechanism of Ciliary Motion

The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
Mechanism of Ciliary Motion01:05

Mechanism of Ciliary Motion

The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...

You might also read

Related Articles

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

Sort by
Same author

Ift43 Controls the Ciliary Levels of Gli2 and Gli3.

bioRxiv : the preprint server for biology·2026
Same author

Pathogenic Pathways and Therapeutic Strategies in Autosomal Dominant Polycystic Kidney Disease (ADPKD).

Journal of cellular signaling·2026
Same author

Activation of the ciliary kinase CDKL5 is mediated by the cyclin-dependent kinase CDK20/LF2 to control flagellar length.

PLoS biology·2025
Same author

DeleteROI for Cleaning CiliaQ Output of Non-ciliary Contamination.

microPublication biology·2025
Same author

Rag GTPases Suppress Renal Cystic Disease by Inhibiting TFEB Independently of mTORC1.

bioRxiv : the preprint server for biology·2025
Same author

Cilia.Pro database of ciliary proteins from vertebrates, <i>Chlamydomonas</i>, and <i>Caenorhabditis</i>.

Molecular biology of the cell·2025

Related Experiment Video

Updated: May 13, 2026

A Graphical User Interface for Software-assisted Tracking of Protein Concentration in Dynamic Cellular Protrusions
08:12

A Graphical User Interface for Software-assisted Tracking of Protein Concentration in Dynamic Cellular Protrusions

Published on: July 11, 2017

Analysis of ciliary membrane protein dynamics using SNAP technology.

John A Follit1, Gregory J Pazour

  • 1Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Methods in Enzymology
|March 19, 2013
PubMed
Summary

Researchers used SNAP technology to track how cells move proteins to the primary cilium, a key structure for sensory functions. This method helps understand protein sorting defects linked to human diseases.

More Related Videos

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations
10:54

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations

Published on: September 17, 2012

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy
10:01

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy

Published on: May 1, 2017

Related Experiment Videos

Last Updated: May 13, 2026

A Graphical User Interface for Software-assisted Tracking of Protein Concentration in Dynamic Cellular Protrusions
08:12

A Graphical User Interface for Software-assisted Tracking of Protein Concentration in Dynamic Cellular Protrusions

Published on: July 11, 2017

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations
10:54

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations

Published on: September 17, 2012

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy
10:01

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy

Published on: May 1, 2017

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Genetics

Background:

  • The primary cilium is crucial for cellular sensory functions.
  • Specific membrane proteins must be sorted to the cilium, a plasma membrane subdomain.
  • Defects in protein sorting to the cilium cause numerous human diseases.

Purpose of the Study:

  • To investigate the mechanisms of protein sorting and trafficking to the ciliary membrane.
  • To understand how cells target proteins to the primary cilium.

Main Methods:

  • Utilized SNAP technology for studying ciliary membrane proteins.
  • Employed pulse-chase analysis to track protein movement through the endomembrane system.
  • Monitored protein translocation onto the cilium.

Main Results:

  • SNAP technology allows detailed observation of protein trafficking to the primary cilium.
  • The study provides a method to analyze the endomembrane system's role in ciliary protein localization.
  • Successfully demonstrated the application of SNAP technology in studying ciliary protein sorting.

Conclusions:

  • The developed method using SNAP technology is effective for studying ciliary protein sorting and trafficking.
  • Understanding these mechanisms is vital for addressing diseases linked to ciliary dysfunction.
  • Further research using this technique can elucidate complex protein transport pathways.