Dual-channel photobleaching FRET microscopy for improved resolution of protein association states in living cells

Andrew H A Clayton, Nectarios Klonis, Stephen Cody, Edouard C Nice

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)

Abstract

Fluorescence resonance energy transfer (FRET) from a donor-labelled molecule to an acceptor-labelled molecule is a useful, proximity-based fluorescence tool to discriminate molecular states on the surface and in the interior of cells. Most microscope-based determinations of FRET yield only a single value, the interpretation of which is necessarily model-dependent. In this paper we demonstrate two new measurements of FRET heterogeneity using selective donor photobleaching in combination with synchronous donor/acceptor detection based on either (1) full kinetic analysis of donor-detected and acceptor-detected donor photobleaching or (2) a simple time-based ratiometric approach. We apply the new methods to study the cell surface distribution of concanavalin A yielding estimates of FRET and non-FRET population distributions, as well as FRET efficiencies within the FRET populations.
Original languageEnglish
Pages (from-to)82 - 90
Number of pages9
JournalEuropean Biophysics Journal
Volume34
Issue number1
Publication statusPublished - 2005

Cite this