Abstract
Single-molecule (sm) fluorescence detection is a powerful method for studying biological events without time and population averaging. Förster (fluorescence) resonance energy transfer (FRET) is a spectroscopic technique in which the efficiency of energy transfer from donor to acceptor molecules is used to determine distances between molecules in the 30-80 Å range. Structural changes in biological molecules or relative motion between two interacting molecules can be detected by a change in FRET. A variant of smFRET is based on total internal reflection (TIR) microscopy, which can be set up in two ways, either using an oil-immersion (objective-type) or a water-immersion (prism-type) lens. This protocol describes the setup for prism-type TIR microscopy (excitation and emission), which has been a major imaging tool for smFRET since it was first introduced.
| Original language | English |
|---|---|
| Pages (from-to) | 1295-1297 |
| Number of pages | 3 |
| Journal | Cold Spring Harbor Protocols |
| Volume | 7 |
| Issue number | 12 |
| DOIs | |
| State | Published - 2012 |