Abstract
Time-domain Fluorescence Lifetime Imaging Microscopy (FLIM) is a remarkable tool to monitor the dynamics of fluorophore-tagged protein domains inside living cells. We propose a Wide-Field Multi-Parameter FLIM method (WFMPFLIM) aimed to monitor continuously living cells under minimum light intensity at a given illumination energy dose. A powerful data analysis technique applied to the WFMP-FLIM data sets allows to optimize the estimation accuracy of physical parameters at very low fluorescence signal levels approaching the lower bound theoretical limit. We demonstrate the efficiency of WFMP-FLIM by presenting two independent and relevant long-term experiments in cell biology: 1) FRET analysis of simultaneously recorded donor and acceptor fluorescence in living HeLa cells and 2) tracking of mitochondrial transport combined with fluorescence lifetime analysis in neuronal processes. © 2011 Vitali et al.
Cite
CITATION STYLE
Vitali, M., Picazo, F., Prokazov, Y., Duci, A., Turbin, E., Götze, C., … Zuschratter, W. (2011). Wide-Field multi-parameter FLIM: Long-term minimal invasive observation of proteins in living cells. PLoS ONE, 6(2). https://doi.org/10.1371/journal.pone.0015820
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.