TY - JOUR
T1 - Rational Design of a Ratiometric Fluorescent Probe Based on Arene-Metal-Ion Contact for Endogenous Hydrogen Sulfide Detection in Living Cells
AU - Kawagoe, Ryosuke
AU - Takashima, Ippei
AU - Usui, Kazuteru
AU - Kanegae, Anna
AU - Ozawa, Yusuke
AU - Ojida, Akio
N1 - Publisher Copyright:
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - We report the design and development of a fluorescent CdII ion complex that is capable of the ratiometric detection of H2S in living cells. This probe exploits the metal-ion-induced emission red shift resulting from direct contact between the aromatic ring of a fluorophore and a metal ion (i.e., arene-metal-ion or "AM" contact). The CdII complex displays a large emission blue shift upon interaction with H2S as the CdII-free ligand is released by the formation of cadmium sulfide. Screening of potential ligands and fluorophores led to the discovery of a pyronine-type probe, 6CdII, that generated a sensitive and rapid ratio value change upon interaction with H2S, without interference from the glutathione that is abundant in the cell. The membrane-impermeable 6CdII was successfully translocated into live cells by using an oligo-arginine peptide and pyrenebutylate as carriers. As such, 6CdII was successfully applied to the ratiometric detection of both exogenous and endogenous H2S produced by the enzymes in living cells, thus demonstrating the utility of 6CdII in biological fluorescence analysis.
AB - We report the design and development of a fluorescent CdII ion complex that is capable of the ratiometric detection of H2S in living cells. This probe exploits the metal-ion-induced emission red shift resulting from direct contact between the aromatic ring of a fluorophore and a metal ion (i.e., arene-metal-ion or "AM" contact). The CdII complex displays a large emission blue shift upon interaction with H2S as the CdII-free ligand is released by the formation of cadmium sulfide. Screening of potential ligands and fluorophores led to the discovery of a pyronine-type probe, 6CdII, that generated a sensitive and rapid ratio value change upon interaction with H2S, without interference from the glutathione that is abundant in the cell. The membrane-impermeable 6CdII was successfully translocated into live cells by using an oligo-arginine peptide and pyrenebutylate as carriers. As such, 6CdII was successfully applied to the ratiometric detection of both exogenous and endogenous H2S produced by the enzymes in living cells, thus demonstrating the utility of 6CdII in biological fluorescence analysis.
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U2 - 10.1002/cbic.201500249
DO - 10.1002/cbic.201500249
M3 - Article
C2 - 26033276
AN - SCOPUS:84937250590
SN - 1439-4227
VL - 16
SP - 1608
EP - 1615
JO - ChemBioChem
JF - ChemBioChem
IS - 11
ER -