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首页> 外文期刊>Bulletin of the Korean Chemical Society >Photophysical Study of 2‐Fluorenyl‐1,2,3‐Triazole‐labeled 2′‐Deoxyuridine and Its Oligonucleotide
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Photophysical Study of 2‐Fluorenyl‐1,2,3‐Triazole‐labeled 2′‐Deoxyuridine and Its Oligonucleotide

机译:2-氟芴基1,2,3-三唑标记的2'-脱氧尿苷及其寡核苷酸的光物理研究

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In this study, we prepared 2‐fluorenyl‐1,2,3‐triazol‐4‐yl‐2′‐deoxyuridine (U FT) and inserted it at the central position of an oligodeoxynucleotide (ODN) to investigate whether the triazole group is an efficient linker between fluorene and uracil. U FT displays different fluorescence intensities and emission maxima in different solvents, indicating its potential for application as an environmentally sensitive probe. Moreover, excimer emission from U FT was observed in water. However, U FT containing ODN did not exhibit selective thermal stability and fluorescence changes upon duplex formation with matched and single‐base mismatched targets. This highlighted the importance of selecting the appropriate linker to connect the fluorophore to the nucleobase when developing such DNA probes.
机译:在这项研究中,我们制备了2-芴基-1,2,3-三唑-4-基-2'-脱氧尿苷(U FT),并将其插入到寡脱氧核苷酸(ODN)的中心位置,以研究三唑基是否为芴和尿嘧啶之间的有效连接子。 U FT在不同的溶剂中显示出不同的荧光强度和最大发射强度,表明其有可能用作环境敏感型探针。此外,在水中观察到来自U FT的准分子发射。但是,含有ODN的U FT在匹配和单碱基错配靶标形成双链体时,没有表现出选择性的热稳定性和荧光变化。这突出了在开发此类DNA探针时选择合适的接头将荧光团连接至核碱基的重要性。

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