期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2004
卷号：101
期号：5
页码：1129-1134
DOI：10.1073/pnas.0308079100
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Zinc is an essential metal ion for human growth and development, the disruption of cellular Zn2+ homeostasis being implicated in several major disorders including Alzheimer's disease, diabetes, and cancer. The molecular mechanisms of Zn2+ physiology and pathology are insufficiently understood, however, owing in part to the lack of tools for measuring changes in intracellular Zn2+ concentrations with high spatial and temporal fidelity. To address this critical need, we have synthesized, characterized, and applied an intracellular fluorescent probe for the ratiometric imaging of Zn2+ based on a tautomeric seminaphthofluorescein platform. Zin-naphthopyr 1 (ZNP1) affords single-excitation, dual-emission ratiometric detection of intracellular Zn2+ through Zn2+-controlled switching between fluorescein and naphthofluorescein tautomeric forms. The probe features visible excitation and emission profiles, excellent selectivity responses for Zn2+ over competing Ca2+ and Mg2+ ions at intracellular concentrations, a dissociation constant (Kd) for Zn2+ of <1 nM, and an 18-fold increase in fluorescence emission intensity ratio ({lambda}624/{lambda}528) upon zinc binding. We demonstrate the value of the ZNP1 platform for biological applications by imaging changes in intracellular [Zn2+] in living mammalian cells. Included is the ratiometric detection of endogenous pools of intracellular Zn2+ after NO-induced release of Zn2+ from cellular metalloproteins. We anticipate that ZNP1 and related probes should find utility for interrogating the biology of Zn2+.
