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用于选择性线粒体成像及动力学研究的设计苯并噻二唑荧光团。

Designed benzothiadiazole fluorophores for selective mitochondrial imaging and dynamics.

作者信息

Carvalho Pedro H P R, Correa Jose R, Guido Bruna C, Gatto Claudia C, De Oliveira Heibbe C B, Soares Thereza A, Neto Brenno A D

机构信息

Laboratory of Medicinal and Technological Chemistry, University of Brasilia (IQ-UnB). Campus Universitário Darcy Ribeiro, CEP 70904970, P.O.Box 4478, Brasilia-DF (Brazil), Fax: (+55) 61-32734149.

出版信息

Chemistry. 2014 Nov 17;20(47):15360-74. doi: 10.1002/chem.201404039. Epub 2014 Oct 21.

Abstract

A series of new rationale designed 2,1,3-benzothiadiazole (BTD) fluorescent derivatives has been synthesized and applied for cellular selective staining of cancer cells in cell-imaging experiments. Four new synthesized BTD derivatives showed only poor or reasonable cellular selection, but with excellent fluorescence intensity and almost no background signal emitting at the blue or green channels. The knowledge gained by analysing their molecular architecture, however, allowed the planning and synthesis of a fluorescent BTD, which was then successfully tested and showed superior mitochondrial selection with outstanding results in bioimaging experiments in living cells. The new marker (named Splendor) was then compared with the commercially available MitoTracker Red (also through co-staining experiments) and showed far better mitochondrial selection, fluorescence intensity and chemical stability. Mitochondrial imaging and tracking (dynamic changes) was possible using Splendor during the whole cellular division cycle. DFT calculations were performed to offer insights into the origin of the chemical- and photostability of BTD derivatives. In addition, molecular docking calculations hint at a potential molecular target for the BTD derivatives in the mitochondrial protein adenine nucleotide translocase, which may explain the mitochondrial selectivity of Splendor versus the other four BTD derivatives.

摘要

一系列新设计的具有合理结构的2,1,3-苯并噻二唑(BTD)荧光衍生物已被合成,并应用于细胞成像实验中对癌细胞进行细胞选择性染色。新合成的四种BTD衍生物仅表现出较差或一般的细胞选择性,但具有出色的荧光强度,并且在蓝色或绿色通道几乎没有背景信号发射。然而,通过分析它们的分子结构所获得的知识,使得能够设计并合成一种荧光BTD,随后该荧光BTD在活细胞的生物成像实验中经过成功测试,显示出卓越的线粒体选择性并取得了出色的结果。然后将新标记物(命名为Splendor)与市售的MitoTracker Red进行比较(同样通过共染色实验),结果表明Splendor在线粒体选择性、荧光强度和化学稳定性方面都远优于MitoTracker Red。在整个细胞分裂周期中,使用Splendor可以实现线粒体成像和跟踪(动态变化)。进行了密度泛函理论(DFT)计算,以深入了解BTD衍生物的化学稳定性和光稳定性的起源。此外,分子对接计算表明BTD衍生物在线粒体蛋白腺嘌呤核苷酸转位酶中存在潜在的分子靶点,这可能解释了Splendor相对于其他四种BTD衍生物的线粒体选择性。

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