Department of Chemistry and Pharmacy, Friedrich-Alexander University (FAU) Erlangen-Nürnberg, 91052, Erlangen, Germany.
Organic Chemistry Department, Institute of Chemistry Martin-Luther-University Halle-Wittenberg, Kurt-Mothes-Straße 2, 06120, Halle, Germany.
Chemistry. 2024 Oct 17;30(58):e202402106. doi: 10.1002/chem.202402106. Epub 2024 Oct 2.
Supramolecular recognition of nucleobases and short sequences is an emerging research field focusing on possible applications to treat many diseases. Controlling the affinity and selectivity of synthetic receptors to target desired nucleotides or short sequences is a highly challenging task. Herein, we elucidate the effect of substituents in the phenyl ring of the anthracene-benzene azacyclophane on the recognition of nucleoside triphosphates (NTPs) and double-stranded DNA. We show that introducing phenyl rings increases the affinity for NTPs 10-fold and implements groove and intercalation binding modes with double-stranded DNA. NMR studies and molecular modeling calculations support the ability of cyclophanes to encapsulate nucleobases as part of nucleotides.
碱基和短序列的超分子识别是一个新兴的研究领域,专注于可能应用于治疗许多疾病。控制合成受体对目标核苷酸或短序列的亲和力和选择性是一项极具挑战性的任务。在此,我们阐明了蒽-苯并氮杂环戊烷中环上取代基对核苷三磷酸 (NTP) 和双链 DNA 识别的影响。我们表明,引入苯环会使 NTP 的亲和力增加 10 倍,并与双链 DNA 形成沟型和嵌入结合模式。NMR 研究和分子建模计算支持了环戊烷将碱基作为核苷酸一部分进行包裹的能力。