Zinc-nucleic acid interaction

被引:222
作者
Aoki, S
Kimura, E
机构
[1] Tokyo Univ Sci, Fac Pharmaceut Sci, Noda, Chiba 2788510, Japan
[2] Hiroshima Univ, Fac Integrated Arts & Sci, Higashihiroshima 7398521, Japan
关键词
D O I
10.1021/cr020617u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A variety of derivatives of Zn2+-cyclen complexes have been designed as prototypes of selective receptors of 'imide'- containing nucleobases, thymine (dT) and uracil (U), in aqueous solution at physiological pH. The Zn2+-cyclen complexes with polyaromatic pendants possess recognition efficiency in terms of Kd on the order of 10 μM in single- and double-stranded DNA (or RNA) to disrupt A-dT hydrogen bonds in double-stranded nucleic acids. A direct correlation was found between the binding of Tat to TAR RNA and up-regulation of HIV-1 mRNA transcription. The potent inhibition of HIV-1 TAR RNA-Tat peptide binding by Zn2+ complexes was described.
引用
收藏
页码:769 / 787
页数:19
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