含三给电子取代基芳基咪唑酮类活细胞脂滴荧光染料的研究

IF 1.7 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Russian Journal of Bioorganic Chemistry Pub Date : 2025-02-12 DOI:10.1134/S1068162025010133
D. I. Rudik, A. R. Gil’vanov, A. Yu. Smirnov, Yu. A. Bogdanova, S. A. Krasnova, M. S. Baranov
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引用次数: 0

摘要

目的:以芳基咪唑酮为基料,制备了一对具有三个给电子基团的荧光染料。方法:采用相应醛的亚胺与随后的[3 + 2]环加成法合成芳基咪唑酮。研究了新化合物的光学性质。用荧光显微镜对活细胞的脂滴进行成像,并用染料标记。结果和讨论:我们发现一对所提出的物质的特征是吸收和发射最大值的显着的色移,以及根据环境的性质,发射最大值的位置的显着变化。我们证明了(Z)-5-(3,5-二(二甲氨基)-4-(乙胺)苄基)-2,3-二甲基-3,5-二氢- 4h -咪唑-4- 1可以染色HeLa Kyoto和Huh 7.5细胞株的脂滴。结论:设计了一种新的基于芳基咪唑酮的选择性荧光染料,可用于活细胞的脂滴标记。
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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Arylidene-Imidazolones with Three Electron-Donating Substituents as Fluorogenic Dyes for Lipid Droplets of Living Cells

Objective: A pair of fluorogenic dyes with three electron-donating groups, based on arylideneimidazolones, is presented. Methods: The formation of imines of the corresponding aldehydes with the subsequent [3 + 2] cycloaddition was used for the synthesis of arylidene-imidazolones. The optical properties of the new compounds were studied. The fluorescence microscopy was used for imaging lipid droplets of the living cells, labeled by the dyes. Results and Discussion: We discovered that a pair of the proposed substances is characterized by a significant bathochromic shift of the absorption and emission maxima, as well as by a noticeable variation of the position of the emission maximum depending on the properties of the environment. We demonstrated that (Z)-5-(3,5-bis(dimethylamino)-4-(ethylamino)benzylidene)-2,3-dimethyl-3,5-dihydro-4H-imidazol-4-one can stain lipid droplets in HeLa Kyoto and Huh 7.5 cell lines. Conclusions: We designed a new selective fluorogenic dye based on arylidene-imidazolones and showed that it can be applicable for lipid droplets labeling in living cells.

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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
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