Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell

Citation
Pih. Bastiaens et A. Squire, Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell, TR CELL BIO, 9(2), 1999, pp. 48-52
Citations number
35
Categorie Soggetti
Cell & Developmental Biology
Journal title
TRENDS IN CELL BIOLOGY
ISSN journal
09628924 → ACNP
Volume
9
Issue
2
Year of publication
1999
Pages
48 - 52
Database
ISI
SICI code
0962-8924(199902)9:2<48:FLIMSR>2.0.ZU;2-T
Abstract
Flourescence lifetime imaging microscopy (FLIM) is a technique in which the mean fluorescence lifetime of a chromophore is measured at each spatially resolvable element of a microscope image. The nanosecond excited-state life time is independent of probe-concentration or light path length but depende nt upon excited-state reactions such as fluorescence resonance energy trans fer (FRET). These properties of fluorescence lifetimes allow exploration of t-he: molecular environment of labelled macromolecules in the interior of c ells. Imaging of fluorescence lifetimes enables biochemical reactions to be followed at each microscopically resolvable location-within the cell.