Related Experiment Video
Updated: Jun 28, 2026

Quantitative Immunofluorescence to Measure Global Localized Translation
Published on: August 22, 2017
A cytoplasmic protein-protein interaction detection method based on reporter translation
Laurence Renaut1, Khalil Bouayadi, Hakim Kharrat
1MilleGen, Immeuble BIOSTEP, 31681 Labege Cedex, France. laurence.renaut@millegen.com
Researchers developed a novel yeast-based system to detect cytoplasmic protein-protein interactions (CPPIs). This technology aids in identifying protein interactions relevant to disease and drug discovery.
Area of Science:
- Biochemistry
- Molecular Biology
- Yeast Genetics
Background:
- Abnormal protein-protein interactions are implicated in various pathologies.
- Targeting these interactions is a key strategy in drug discovery.
- Existing methods for detecting cytoplasmic interactions have limitations.
Purpose of the Study:
- To present a new technology for detecting cytoplasmic protein-protein interactions (CPPIs) in a yeast system.
- To provide a tool for characterizing proteins and identifying interaction partners.
- To facilitate drug discovery applications by enabling the study of CPPIs.
Main Methods:
- A yeast-based system was engineered for interaction detection.
- The system relies on the sequestration of a translation termination factor.
- Sequestration of the factor allows translation of a reporter gene with a premature stop codon.
Main Results:
- The developed system successfully detects cytoplasmic protein-protein interactions.
- The technology leverages the inhibition of a translation termination factor's activity.
- Successful translation of the reporter gene indicates interaction.
Conclusions:
- The novel CPPI detection system offers a valuable tool for biological research.
- This system can be applied to protein characterization and interaction mapping.
- The technology holds promise for advancing drug discovery efforts targeting CPPIs.
More Related Videos
09:52An In Vitro Single-Molecule Imaging Assay for the Analysis of Cap-Dependent Translation Kinetics
Published on: September 15, 2020
07:03Pulldown Assay Coupled with Co-Expression in Bacteria Cells as a Time-Efficient Tool for Testing Challenging Protein-Protein Interactions
Published on: December 23, 2022
Related Concept Videos
Ribosome Profiling
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
Reporter Genes
Commonly used reporter...
Protein Dynamics in Living Cells
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...
Cotranslational Protein Translocation
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...