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Synthesis and properties of peptide nucleic acid labeled at the N-terminus with HiLyte Fluor 488 fluorescent dye

机译:HiLyte Fluor 488荧光染料在N端标记的肽核酸的合成和性质

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摘要

Fluorescently labeled peptide nucleic acids (PNAs) are important tools in fundamental research and biomedical applications. However, synthesis of labeled PNAs, especially using modern and expensive dyes, is less explored than similar preparations of oligonucleotide dye conjugates. Herein, we present a simple procedure for labeling of the PNA N-terminus with HiLyte Fluor 488 as the last step of solid phase PNA synthesis. A minimum excess of 1.25 equiv of activated carboxylic acid achieved labeling yields close to 90% providing a good compromise between the price of dye and the yield of product and significant improvement over previous literature procedures. The HiLyte Fluor 488-labeled PNAs retained the RNA binding ability and in live cell fluorescence microscopy experiments were brighter and significantly more photostable than PNA labeled with carboxyfluorescein. In contrast to fluorescein-labeled PNA, the fluorescence of PNAs labeled with HiLyte Fluor 488 was independent of pH in the biologically relevant range of 5–8. The potential of HiLyte Fluor 488-labeling for studies of PNA cellular uptake and distribution was demonstrated in several cell lines.
机译:荧光标记的肽核酸(PNA)是基础研究和生物医学应用中的重要工具。但是,与类似的寡核苷酸染料偶联物制备方法相比,探索标记的PNA尤其是使用现代昂贵的染料进行合成的研究较少。在这里,我们提出了一个简单的程序,用HiLyte Fluor 488标记PNA N末端,作为固相PNA合成的最后一步。最小过量1.25当量的活化羧酸可达到接近90%的标记收率,这在染料价格和产品收率之间提供了一个很好的折衷方案,并且比以前的文献方法有了显着改进。 HiLyte Fluor 488标记的PNA保留了RNA结合能力,并且在活细胞荧光显微镜实验中比用羧基荧光素标记的PNA更亮,并且光稳定性更高。与荧光素标记的PNA相比,HiLyte Fluor 488标记的PNA的荧光在5-8的生物学相关范围内与pH无关。在几种细胞系中证明了HiLyte Fluor 488标记用于研究PNA细胞摄取和分布的潜力。

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