基于 N-脒基硫脲的高选择性、高灵敏度荧光化学传感器,用于检测 Zn2+ 离子和细胞成像:质膜检测的潜在应用

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Crystal Liu , Katlin Ricks , Muneeb Akhtar , Sergio Mendez , Ian Lian , Zhi-Fo Guo
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引用次数: 0

摘要

开发了一种 "开启式 "荧光传感器 L,用于在生物环境中选择性地检测 Zn2+ 离子。该传感器对 Zn2+ 离子有特异性反应,检测限为 39 nM。通过滴定和约伯图分析证实,所形成的复合物具有 2:1 的化学计量比(L:Zn2+)。该传感器对 Zn2+ 的选择性强于其他金属离子,显示出强大的结合亲和力,同时有效减少了重金属的干扰。傅立叶变换红外光谱(FT-IR)、质子核磁共振(1H NMR)滴定、质谱分析(MS)和密度泛函理论(DFT)计算验证了这一识别过程。在生理 pH 值为 7.0-7.5 的范围内,当与 Zn2+ 离子相互作用时,荧光强度达到最大。此外,在 HEK293 细胞中成功进行的成像实验凸显了该传感器作为监测质膜相互作用的强大工具的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Highly selective and sensitive N-amidothiourea-based fluorescence chemosensor for detecting Zn2+ ions and cell Imaging: Potential applications for plasma membrane detection

Highly selective and sensitive N-amidothiourea-based fluorescence chemosensor for detecting Zn2+ ions and cell Imaging: Potential applications for plasma membrane detection
A “turn-on” fluorescent sensor L was developed for the selective detection of Zn2+ ions in biological settings. This sensor exhibited a specific response to Zn2+ ions, with a detection limit of 39 nM. Analyses through titration and Job’s plot confirmed that the formed complex has a 2:1 stoichiometry (L: Zn2+). The sensor displayed strong selectivity for Zn2+ over other metal ions, demonstrating a robust binding affinity while effectively reducing interference from heavy metals. The identification process was validated by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (1H NMR) titrations, mass spectrometry (MS), and Density Functional Theory (DFT) calculations. Maximum fluorescence intensity was achieved upon interaction with Zn2+ ions within a physiological pH range of 7.0–7.5. Moreover, successful imaging experiments in HEK293 cells highlighted the sensor’s potential as a powerful tool for monitoring interactions at the plasma membrane.
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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