Related Experiment Video
Updated: Aug 9, 2026

19:05
Measuring TCR-pMHC Binding In Situ using a FRET-based Microscopy Assay
Published on: October 30, 2015
C-terminal fluorescence labeling of proteins for interaction studies on the single-molecule level
Christian F W Becker1, Ralf Seidel, Michael Jahnz
1Max-Planck-Institut für molekulare Physiologie, Physikalische Biochemie, Otto-Hahn Strasse 11, 44227 Dortmund, Germany. christian.becker@mpi-dortmund.mpg.de
Chembiochem : a European Journal of Chemical Biology
|April 12, 2006
Abstract
No abstract available in PubMed .
Related Concept Videos
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...
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...
Total Internal Reflection Fluorescence Microscopy
Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.

