基于阿兹内酯探针的G4 DNA结构荧光发光研究

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Annyesha Biswas, Nitesh Ayare, Y. Dilnawaj, Vipin Kumar Mishra and P. I. Pradeepkumar*, 
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引用次数: 0

摘要

富含g的DNA和RNA序列可以形成g -四重体(G4)结构,调节无数的生物过程。因此,有必要了解G4s在无细胞条件和细胞环境下的结构拓扑、位置和功能。在本研究中,我们报道了三种基于AZL1-3的小分子荧光探针,它们显著地照亮了c-MYC、c-KIT1和线粒体HRCC G4 dna的平行拓扑结构(约65 - 135倍)。铅探针AZL1通过进入5 ‘和3 ’ - g四重奏,与c-KIT1 G4 DNA表现出2:1的结合化学计量。由于与线粒体G4 dna的弱共定位以及与脂滴的强共定位,它在HeLa细胞的细胞质中显示有限的细胞毒性和荧光发光。这些结果表明,基于阿兹内酯的探针是在无细胞环境中检测G4结构的有用工具,并且可以进一步设计用于潜在的生物成像和诊断应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fluorescence Light-Up of G4 DNA Structures Using Azlactone-Based Probes

Fluorescence Light-Up of G4 DNA Structures Using Azlactone-Based Probes

G-rich sequences of DNA and RNA can form G-quadruplex (G4) structures, modulating a myriad of biological processes. Thus, it is imperative to understand the structural topologies, location, and function of G4s under cell-free conditions and in the cellular milieu. In the present study, we report three small-molecule fluorescent probes based on azlactones (AZL1-3) that significantly light up (∼65–135-fold) the parallel topology of the c-MYC, c-KIT1, and mitochondrial HRCC G4 DNAs. The lead probe AZL1 exhibits a 2:1 binding stoichiometry with c-KIT1 G4 DNA by accessing the 5′ and 3′-G-quartets. It shows limited cytotoxicity and exhibits fluorescence light-up in the cytoplasm of the HeLa cells due to weak colocalization with the mitochondrial G4 DNAs along with strong colocalization with lipid droplets. These results demonstrate that azlactone-based probes are useful tools to sense G4 structures in a cell-free environment and could be further engineered for potential bioimaging and diagnostic applications.

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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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