Wide-Field multi-parameter FLIM: Long-term minimal invasive observation of proteins in living cells

33Citations
Citations of this article
55Readers
Mendeley users who have this article in their library.

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

APA

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.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free