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Molecular recognition of AT-DNA sequences by the induced CD pattern of dibenzotetraaza14annulene (DBTAA) - adenine derivatives

机译:通过诱导的二苯并四氮杂14环戊烯(DBTAA)-腺嘌呤衍生物的CD模式对AT-DNA序列进行分子识别

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摘要

An investigation of the interactions of two novel and several known DBTAA–adenine conjugates with double-stranded DNA and RNA has revealed the DNA/RNA groove as the dominant binding site which is in contrast to the majority of reviously studied DBTAA analogues (DNA/RNA intercalators). Only DBTAA–propyladenine conjugates revealed the molecular recognition of AT-DNA by an ICD band pattern 300 nm, whereas significant ICD bands did not appear for other ds-DNA/RNA. A structure–activity relation for the studied series of compounds showed that the essential structural features for the ICD recognition are a) the presence of DNA-binding appendages (adenine side chain and positively charged side chain) on both DBTAA side chains, and b) the presence of a short propyl linker, which does not support intramolecular aromatic stacking between DBTAA and adenine. The observed AT-DNA-ICD pattern differs from previously reported ss-DNA (poly dT) ICD recognition by a strong negative ICD band at 350 nm, which allows for the dynamic differentiation between ss-DNA (poly dT) and coupled ds-AT-DNA.
机译:对两种新颖的和几种已知的DBTAA-腺嘌呤结合物与双链DNA和RNA的相互作用的研究表明,DNA / RNA沟是主要的结合位点,这与大多数先前研究过的DBTAA类似物(DNA / RNA)相反嵌入剂)。只有DBTAA-丙基腺嘌呤结合物可以通过> 300 nm的ICD谱带显示出对AT-DNA的分子识别,而其他ds-DNA / RNA却没有出现明显的ICD谱带。对所研究化合物系列的结构-活性关系表明,ICD识别的基本结构特征是:a)两个DBTAA侧链上都存在DNA结合附件(腺嘌呤侧链和带正电的侧链),以及b)存在短的丙基接头,该接头不支持DBTAA和腺嘌呤之间的分子内芳族堆积。观察到的AT-DNA-ICD模式不同于先前报道的ss-DNA(poly dT)ICD识别,在350 nm处有很强的ICD负带,这使得ss-DNA(poly dT)和耦合的ds-AT之间可以动态区分。 -脱氧核糖核酸。

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