抄録
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.
本文言語 | English |
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ページ(範囲) | 1608-1615 |
ページ数 | 8 |
ジャーナル | ChemBioChem |
巻 | 16 |
号 | 11 |
DOI | |
出版ステータス | Published - 2015 7月 1 |
外部発表 | はい |
ASJC Scopus subject areas
- 生化学
- 分子医療
- 分子生物学
- 有機化学