Related Experiment Video
Updated: Apr 27, 2026

08:32
Conducting Multiple Imaging Modes with One Fluorescence Microscope
Published on: October 28, 2018
9.4K
The bright future of single-molecule fluorescence imaging
Manuel F Juette1, Daniel S Terry1, Michael R Wasserman1
1Department of Physiology and Biophysics, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10065, United States.
Current Opinion in Chemical Biology
|June 24, 2014
Summary
Ultra-stable organic fluorophores are key for multi-color single-molecule Förster resonance energy transfer (smFRET) studies. These advanced labels enable precise analysis of biomolecular interactions and dynamics, unlocking new biological insights.
Area of Science:
- Biophysics
- Molecular Biology
- Biochemistry
Background:
- Single-molecule Förster resonance energy transfer (smFRET) is a vital technique for studying biomolecular dynamics.
- Current smFRET applications are increasingly moving towards complex biological systems like living cells.
- Advanced fluorescent labels are crucial for overcoming limitations in spectral separation, time resolution, and observation duration.
Purpose of the Study:
- To highlight the critical role of advanced fluorescent labels in multi-color smFRET.
- To discuss the development of ultra-stable organic fluorophores for enhanced smFRET experiments.
- To underscore the potential of improved fluorophores for biological discoveries.
Main Methods:
- Development of ultra-stable organic fluorophores across the visible spectrum.
- Integration of these fluorophores into multi-color smFRET experimental designs.
- Advanced data analysis techniques to interpret smFRET signals.
Main Results:
- Strategies for creating long-lasting, non-fluctuating organic fluorophores have been developed.
- These fluorophores meet the stringent demands for multi-color smFRET.
- Progress in fluorophore development is enabling more sophisticated smFRET studies.
Conclusions:
- Ultra-stable fluorophores are essential for advancing multi-color smFRET.
- These labels facilitate the detailed study of biomolecular interactions and conformational changes.
- Future smFRET studies with improved fluorophores promise unprecedented biological insights.
Related Concept Videos
Super-resolution Fluorescence Microscopy
12.3K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
12.3K
Total Internal Reflection Fluorescence Microscopy
11.0K
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.
11.0K

