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

1.9K
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...
1.9K
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

1.8K
Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
1.8K

You might also read

Related Articles

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

Sort by
Same author

NECAP antagonizes light-induced Rhodopsin-1 internalization to promote photoreceptor homeostasis.

bioRxiv : the preprint server for biology·2026
Same author

Approaches to deorphanize secretome: Classical, computational, and next generation strategies to reveal ligand-receptor networks.

EXO : beyond the cell·2026
Same author

Conserved principles of central carbon partitioning in Hippo-Yorkie-driven <i>Drosophila</i> gut tumors.

bioRxiv : the preprint server for biology·2026
Same author

LIVIA: a browser-based tool for assessing and visualizing predicted protein interactions.

bioRxiv : the preprint server for biology·2026
Same author

Genome-wide CRISPR knockout cell screening platform for the disease vector tick species <i>Ixodes scapularis</i>.

bioRxiv : the preprint server for biology·2026
Same author

Liver-derived ceramides link metabolism to tissue wasting in cancer cachexia.

The Journal of clinical investigation·2026
Same journal

ZNRF3 and RNF43 are active monomeric E3 ubiquitin ligases that self-associate.

Science signaling·2026
Same journal

Allosteric ligands with distinct properties uncover tissue-specific physiological regulation mediated by free fatty acid receptor 2.

Science signaling·2026
Same journal

Diacylglycerol kinase ζ in B lymphocytes supports CD40-mediated immune synapse formation, mTORC1 signaling, and plasma cell fate.

Science signaling·2026
Same journal

The APC/C adaptor Cdh1 stabilizes STING to potentiate innate immune activation in renal cell carcinoma.

Science signaling·2026
Same journal

Fattening mother's milk with oxytocin.

Science signaling·2026
Same journal

Virion display reveals MD-1 as an endogenous agonist for the orphan receptor GPRC5B.

Science signaling·2026
See all related articles

Related Experiment Video

Updated: May 1, 2026

Fluorescence detection methods for microfluidic droplet platforms
14:16

Fluorescence detection methods for microfluidic droplet platforms

Published on: December 10, 2011

24.8K

Visualizing and manipulating temporal signaling dynamics with fluorescence-based tools.

David P Doupé1, Norbert Perrimon

  • 11Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

Science Signaling
|April 3, 2014
PubMed
Summary
This summary is machine-generated.

Understanding cellular signal transduction networks requires studying information flow dynamics. New fluorescence and optogenetic tools allow real-time analysis of signaling pathways in living cells, revealing how temporal dynamics impact cell fate.

More Related Videos

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
08:55

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

Published on: December 29, 2017

11.0K
Temporal Quantification of MAPK Induced Expression in Single Yeast Cells
07:59

Temporal Quantification of MAPK Induced Expression in Single Yeast Cells

Published on: October 4, 2013

7.9K

Related Experiment Videos

Last Updated: May 1, 2026

Fluorescence detection methods for microfluidic droplet platforms
14:16

Fluorescence detection methods for microfluidic droplet platforms

Published on: December 10, 2011

24.8K
Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
08:55

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

Published on: December 29, 2017

11.0K
Temporal Quantification of MAPK Induced Expression in Single Yeast Cells
07:59

Temporal Quantification of MAPK Induced Expression in Single Yeast Cells

Published on: October 4, 2013

7.9K

Area of Science:

  • Cellular Biology
  • Systems Biology
  • Molecular Biology

Background:

  • Signal transduction understanding has evolved from linear pathways to complex networks.
  • Probing information flow dynamics within these networks remains a significant technical challenge.
  • Temporal dynamics' role in eliciting distinct cellular outcomes and influencing cell fate is largely unknown.

Purpose of the Study:

  • To provide an overview of the importance of temporal dynamics in cellular regulation.
  • To introduce fluorescence-based reporters and optogenetic regulators for analyzing signaling dynamics.
  • To highlight studies demonstrating the utility of these tools in probing information flow.

Main Methods:

  • Utilizing genome-wide proteomic and RNA interference approaches.
  • Employing fluorescence-based reporters for real-time signaling analysis.
  • Leveraging optogenetic regulators for precise control of pathway activity.

Main Results:

  • Demonstrated the critical role of signal dynamics in determining cellular responses.
  • Showcased the application of novel tools in *Caenorhabditis elegans* sensory neurons.
  • Highlighted findings from studies using cultured mammalian cells.

Conclusions:

  • Temporal dynamics are crucial for cellular regulation and signaling network function.
  • Advanced tools like fluorescence reporters and optogenetics are essential for dissecting signaling dynamics.
  • Future research can further elucidate how signal dynamics govern cell fate decisions.