Simultaneous visualization of lipid droplets and tracking of the endogenous hypochlorous acid in psoriatic mice models with a novel fluorescent probe in a wash-free fashion.

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Bioorganic Chemistry Pub Date : 2024-12-01 Epub Date: 2024-11-16 DOI:10.1016/j.bioorg.2024.107967
Xuan Zhao, Xiaoxue Hu, Longxuan Li, Yuanping Liu, Boshuang Song, Yuzhi Li, Zhixing Cao, Houcheng Zhou, Cheng Peng, Yun Deng, Yuyu Fang
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Abstract

Psoriasis is an autoimmune inflammation-related disease accompanied by a variety of complications. Reactive oxygen species (ROS) are modulators of inflammation, and their excessive production caused by oxidative/anti-oxidative imbalance has been observed in psoriatic patients. Hypochlorous acid (HOCl) is a ROS produced by myeloperoxidase (MPO) from chloride ions (Cl-) and hydrogen peroxide (H2O2). Endogenous HOCl has recently been studied as a potential biomarker of psoriasis underlying the necessity for the development of efficient analytical tools for its detection and real time monitoring. Herein, we designed a novel highly sensitive and selective coumarin-based fluorescent probe for HOCl detection, named CN2-CF3-S. The probe itself featured negligible fluorescence because of the heavy atom effect of the thiocarbonyl group. However, upon responding to HOCl a conversion to sulfur-free derivative CN2-CF3-O occurs, resulting in a dramatical fluorescent enhancement setting the detection limit for HOCl of 3.2 nM. The HOCl-recognition mechanism could be ascribed to the HOCl-triggered oxidative desulfurization process that agrees with liquid chromatography-mass spectrometry (LC-MS) analysis and density functional theory (DFT) computations. The probe's design incorporated a synergistic combination of two structural features for efficient lipid droplets (LDs)-targeting imaging. An efficient push-pull system reinforced by the presence of two strongly electron-donating dimethylamino groups equipped CN2-CF3-O with pronounced solvatochromism realized through the enhanced blue-shifted emission in non-polar media. Meanwhile, the presence of trifluormethylphenyl moiety at the acceptor side led to an increased lipophilicity. The CN2-CF3-S probe has been successfully utilized to track the endogenous HOCl in cells and on skin of the psoriatic mice in a wash-free manner. As a result, we have demonstrated that the concentration of HOCl in skin might correlate positively with the degree of inflammation in psoriasis. Thus, CN2-CF3-S constitutes the first example of LDs-imaging fluorescent probe for detecting the psoriasis-linked HOCl, offering a convenient tool for further in-depth investigation of psoriasis pathophysiology.

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利用新型荧光探针以免洗方式同时观察银屑病小鼠模型中的脂滴并追踪内源性次氯酸。
银屑病是一种自身免疫性炎症相关疾病,伴有多种并发症。活性氧(ROS)是炎症的调节剂,在银屑病患者中观察到,氧化/抗氧化失衡导致活性氧产生过多。次氯酸(HOCl)是髓过氧化物酶(MPO)从氯离子(Cl-)和过氧化氢(H2O2)中产生的一种 ROS。内源性 HOCl 最近被研究为银屑病的潜在生物标志物,这就要求开发高效的分析工具对其进行检测和实时监控。在此,我们设计了一种新型的高灵敏度、高选择性香豆素基荧光探针,用于检测 HOCl,命名为 CN2-CF3-S。由于硫代羰基的重原子效应,探针本身的荧光可以忽略不计。然而,在与 HOCl 发生反应时,会转化为无硫衍生物 CN2-CF3-O,从而显著增强荧光,将 HOCl 的检测限设定为 3.2 nM。HOCl 的识别机制可归因于 HOCl 触发的氧化脱硫过程,这与液相色谱-质谱(LC-MS)分析和密度泛函理论(DFT)计算相吻合。探针的设计融合了两种结构特征的协同组合,可实现高效的脂滴(LDs)靶向成像。两个强电子捐赠二甲基氨基的存在加强了高效的推拉系统,使 CN2-CF3-O 在非极性介质中通过增强的蓝移发射实现了明显的溶解变色。同时,受体侧三氟甲基苯基分子的存在增加了亲油性。我们成功地利用 CN2-CF3-S 探针以免清洗的方式跟踪了细胞和银屑病小鼠皮肤中的内源性 HOCl。结果表明,皮肤中 HOCl 的浓度可能与银屑病的炎症程度呈正相关。因此,CN2-CF3-S 是首个用于检测与银屑病相关的 HOCl 的 LDs-imaging 荧光探针,为进一步深入研究银屑病病理生理学提供了便捷的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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