Year: 2002
Type: article
Abstract: Recently, fluorescence resonance energy transfer (FRET) and fluorescence lifetime imaging microscopy (FLIM) have been the buzzwords for monitoring protein-protein interactions in living cells.These methodologies provide higher temporal (< 1 ns) and spatial resolution (1-10 nm) than near field microscopy (50 nm).FRET microscopy is an excellent method for imaging the structure and localization of proteins under physiological conditions, since other methods, including X-ray diffraction and electron microscopy, require the specimens to be fixed.
Source: BioTechniques
DOI: 10.2144/02326im01
Institution: University of Virginia
Language: English
Subfield: Biophysics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $1,415
Funder: W. M. Keck Foundation
OpenAlex ID: W160352383
