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 objective-type TIR microscopy (excitation), including setup of the laser beam and epifluorescence microscopy, and conversion of the latter into TIR.
Original language | English |
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Pages (from-to) | 1189-1191 |
Number of pages | 3 |
Journal | Cold Spring Harbor Protocols |
Volume | 7 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2012 |