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From the Cover: A tautomeric zinc sensor for ratiometric fluorescence imaging: Application to nitric oxide-induced release of intracellular zinc

机译:从封面开始:用于比例荧光成像的互变异构锌传感器:在一氧化氮诱导的细胞内锌释放中的应用

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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 (λ624/λ528) 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+.
机译:锌是人类生长发育必不可少的金属离子,细胞内Zn 2 + 体内稳态的破坏与多种主要疾病有关,包括阿尔茨海默氏病,糖尿病和癌症。 Zn 2 + 生理和病理学的分子机制尚不充分了解,部分原因是缺乏用于测量高空间内细胞内Zn 2 + 浓度变化的工具和时间保真度。为了满足这一关键需求,我们已经合成,表征并应用了基于互变异构半萘荧光素平台的Zn 2 + 比例成像的细胞内荧光探针。 Zin-naphthopyr 1(ZNP1)通过荧光素和萘荧光素互变异构形式之间的Zn 2 + 控制切换,可对细胞内Zn 2 + 进行单激发,双发射比率检测。该探针具有可见的激发和发射曲线,在细胞内浓度下对竞争的Ca 2 + 和Mg 2 + 离子具有出色的Zn 2 + 选择性响应,Zn 2 + 的解离常数(Kd)<1 nM,锌结合后荧光发射强度比(λ624/λ528)增加18倍。通过成像活哺乳动物细胞内细胞内[Zn 2 + ]的变化,我们证明了ZNP1平台对于生物学应用的价值。 NO诱导细胞金属蛋白释放Zn 2 + 后内源性池内Zn 2 + 的比例检测。我们预期ZNP1及其相关探针应可用于研究Zn 2 + 的生物学特性。

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