Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Red-edge anisotropy microscopy enables dynamic imaging of homo-FRET between green fluorescent proteins in cells

Item Type:Article
Title:Red-edge anisotropy microscopy enables dynamic imaging of homo-FRET between green fluorescent proteins in cells
Creators Name:Squire, A., Verveer, P.J., Rocks, O. and Bastiaens, P.I.
Abstract:Steady-state fluorescence anisotropy measurements can be used to detect fluorescence resonance energy transfer (FRET) between identical fluorophores (homo-FRET). However, the contribution of homo-FRET to the steady-state anisotropy must be discerned from those due to the orientational distribution and rotational diffusion, which so far has required photobleaching controls, largely precluding dynamic measurements in live cells. We describe a variation of steady-state anisotropy microscopy in which the contribution of homo-FRET is dynamically isolated from the total anisotropy by exploiting the loss of energy transfer that occurs at red-edge excitation. Excitation of enhanced green fluorescent protein (EGFP) at the red-edge of its absorption band shows the shift in the emission spectrum compared to main-band excitation that is characteristic for photo-selection of static low energy S(0)-S(1) transitions that fail to exhibit FRET. An experimental setup for steady-state fluorescent anisotropy microscopy is described that can be used to acquire anisotropy images in live cells at main-band and red-edge excitation of EGFP. We demonstrate in live cells homo-FRET suppression of protein fusion constructs that consist of two and three EGFP molecules connected by short linkers. This methodology represents a novel approach for the dynamic measurement of homo-FRET in live cells that will be of utility in the biological sciences to detect oligomerization and concentration dependent interactions between identically labeled molecules.
Keywords:Anisotropy, Tumor Cell Line, Fluorescence Resonance Energy Transfer, Green Fluorescent Proteins, Fluorescence Microscopy, Protein Conformation
Source:Journal of Structural Biology
ISSN:1047-8477
Publisher:Elsevier
Volume:147
Number:1
Page Range:62-69
Date:July 2004
Official Publication:https://doi.org/10.1016/j.jsb.2003.10.013
PubMed:View item in PubMed

Repository Staff Only: item control page

Open Access
MDC Library