新型咔唑-苯并吡喃基荧光探针识别ONOO-及其应用。

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Peng Wang, Qian Wang, Yana Tao, Yuan Ji, Min Fang, Cun Li, Weiju Zhu
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引用次数: 0

摘要

在本研究中,我们在n -丁基咔唑的3位上引入苯并吡喃丙二腈,在n -丁基咔唑的6位上引入硼酸pinacol结构,成功地合成了一种比色荧光荧光探针CBB。具有明显Stokes位移(146 nm)的探针CBB对ONOO-具有高选择性和灵敏度。该探针CBB可通过紫外-可见和荧光光谱技术特异性鉴定ONOO-。将ONOO-加入到CBB溶液中,溶液的颜色在日光下由橙色变为无色,在365nm紫外灯下由粉红色变为蓝色,使这些颜色很容易被肉眼识别。通过1H NMR,质谱(MS)和密度泛函理论(DFT)计算验证了识别机制。此外,细胞成像实验表明,CBB通过荧光共聚焦显微镜有效捕获HeLa细胞红色和蓝色通道的荧光信号,成功识别了这些细胞内的外源性ONOO-。这些结果表明,探针CBB对ONOO-具有较强的监测能力,为相关领域的研究和应用提供了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A New Fluorescent Probe based on Carbazole-Benzopyranyl for the Recognition of ONOO- and its Application.

In this study, we successfully synthesized a colorimetric and photoluminescent fluorescent probe CBB by introducing benzopyran malononitrile at the 3-position of N-butylcarbazole and pinacol borate structure at the 6-position of N-butylcarbazole. The probe CBB characterized by a substantial Stokes shift (146 nm) demonstrates high selectivity and sensitivity to ONOO-. The probe CBB can specifically identify ONOO- by UV-Vis and fluorescence spectroscopic techniques. When ONOO- is added to the solution of CBB, the solution's color transitions from orange to colorless in daylight, and from pink to blue under a 365 nm UV lamp, making these can be easily recognized by the naked eye. The recognition mechanism was validated using 1H NMR, mass spectrometry (MS) and density functional theory (DFT) calculations. In addition, cell imaging experiments demonstrated that CBB effectively captured the fluorescence signals in both the red and blue channels of HeLa cells through fluorescence confocal microscopy, successfully identifying exogenous ONOO- within these cells. These results show that the probe CBB possesses strong monitoring capabilities for ONOO-, offering new opportunities for research and application in related fields.

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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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