| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1305901 | Inorganic Chemistry Communications | 2011 | 4 Pages |
The integration of bis(pyridin-2-ylmethyl)amine (BPA) with 8-sulfonamidoquinoline (SQ) resulted in a new fluorescent Zn2+ sensor of 1:1 binding stoichiometry. The synergic Zn2+ coordination of BPA and SQ motifs provides the sensor the advantage over TSQ and its analogues in discriminating mobile Zn2+ from the bound Zn2+ of unoccupied coordination sites in living systems. Its pH-independent Zn2+-enhanced emission in physiological condition and cell permeability make it an effective intracellular Zn2+ imaging agent. This sensor profits also from its confirmed Golgi-preferential affinity, and its pH-independent Zn2+ response in physiological pH range provides it the advantages over other xanthenone-based sensors.
Graphical AbstractThe BPA incorporation in 8-sulfonamidoquinoline provides a novel Zn2+ fluorescent sensor BPSQ with 1:1 Zn2+ binding stoichiometry. It possesses the pH-independent sensing behavior, cell permeability and the higher ability than TSQ in discriminating the mobile Zn2+ from those of unoccupied coordination sites in biological systems.Figure optionsDownload full-size imageDownload as PowerPoint slideResearch Highlights► A new sulfonamidoquinoline-based Zn2+ fluorescent sensor. ► The 1:1 Zn2+ binding stoichiometry other than 2:1 of normal TSQ analogues. ► The intracellular Zn2+ imaging ability and Golgi preference. ► Reducing the interference of the partially coordinated Zn2+ with the mobile Zn2+.
