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Single Fluorescent Probe Responds to H2O2, NO, and H2O2/NO with Three Different Sets of Fluorescence Signals

Author:
Yuan, Lin, Lin, Weiying, Xie, Yinan, Chen, Bin, Zhu, Sasa
Source:
Journal of the American Chemical Society 2012 v.134 no.2 pp. 1305-1315
ISSN:
1520-5126
Subject:
biochemical compounds, fluorescence, fluorescent dyes, hydrogen peroxide, image analysis, macrophages, monitoring, nitric oxide, oxidative stress, second messengers, smooth muscle, spectral analysis
Abstract:
Hydrogen peroxide (H₂O₂) acts as a signaling molecule in a wide variety of signaling transduction processes and an oxidative stress marker in aging and disease. However, excessive H₂O₂ production is implicated with various diseases. Nitric oxide (NO) serves as a secondary messenger inducing vascular smooth muscle relaxation. However, mis-regulation of NO production is associated with various disorders. To disentangle the complicated inter-relationship between H₂O₂ and NO in the signal transduction and oxidative pathways, fluorescent reporters that are able to display distinct signals to H₂O₂, NO, and H₂O₂/NO are highly valuable. Herein, we present the rational design, synthesis, spectral properties, and living cell imaging studies of FP-H₂O₂-NO, the first single-fluorescent molecule, that can respond to H₂O₂, NO, and H₂O₂/NO with three different sets of fluorescence signals. FP-H₂O₂-NO senses H₂O₂, NO, and H₂O₂/NO with a fluorescence signal pattern of blue–black–black, black–black–red, and black–red–red, respectively. Significantly, we have further demonstrated that FP-H₂O₂-NO, a single fluorescent probe, is capable of simultaneously monitoring endogenously produced NO and H₂O₂ in living macrophage cells in multicolor imaging. We envision that FP-H₂O₂-NO will be a unique molecular tool to investigate the interplaying roles of H₂O₂ and NO in the complex interaction networks of the signal transduction and oxidative pathways. In addition, this work establishes a robust strategy for monitoring the multiple ROS and RNS species (H₂O₂, NO, and H₂O₂/NO) using a single fluorescent probe, and the modularity of the strategy may allow it to be extended for other types of biomolecules.
Agid:
5385429