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新型PRODAN标记核苷作为碱基区分荧光探针的开发。

Development of novel PRODAN-labeled nucleosides as base-discriminating fluorescent probes.

作者信息

Tainaka Kazuki, Ikeda Shuji, Tanaka Kazuo, Nishiza Ken-ichiro, Fujiwara Yoshimasa, Okamoto Akimitsu, Saito Isao

机构信息

Frontier Research System, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.

出版信息

Nucleic Acids Symp Ser (Oxf). 2006(50):133-4. doi: 10.1093/nass/nrl066.

Abstract

We have developed a PRODAN-labeled uridine ((PDN)U), which contains a polarity-sensitive chromophore at the C-5 position of uracil. This paper describes the synthesis and fluorescent properties of oligodeoxy-nucleotides (ODNs) containing PRODAN-labeled nucleosides ((PDN)C, (PDN)A, and (PDN)G). PRODAN chromophore was attached to cytosine at the C-5 position and to purine bases at the C-8 position to extend into the major groove. When BDF probes containing a PRODAN-labeled nucleoside hybridize with a "full-matched" ODN, the fluorescence spectrum showed a strong emission around 520 nm on 450 nm excitation. In contrast, when PRODAN-labeled nucleoside analogs form a "mismatched" base pair, the fluorescence was weaker.

摘要

我们开发了一种PRODAN标记的尿苷((PDN)U),它在尿嘧啶的C-5位含有一个极性敏感发色团。本文描述了含有PRODAN标记核苷((PDN)C、(PDN)A和(PDN)G)的寡脱氧核苷酸(ODN)的合成及荧光特性。PRODAN发色团连接在胞嘧啶的C-5位和嘌呤碱基的C-8位,延伸至大沟中。当含有PRODAN标记核苷的BDF探针与“完全匹配”的ODN杂交时,在450nm激发下,荧光光谱在520nm左右显示出强烈发射。相反,当PRODAN标记的核苷类似物形成“错配”碱基对时,荧光较弱。

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