Interaction between a fluoroquinolone derivative KG022 and RNAs: effect of the bulged residues.

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rika Ichijo, Gota Kawai
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引用次数: 0

Abstract

To progress the RNA-binding small molecule drug discovery, the specific interaction between RNAs having a single bulge and a fluoroquinolone derivative, KG022, was analyzed by NMR spectroscopy. In our previous work, it was found that KG022 is located between the two base pairs at the 3' and 5' side of the bulged residue. KG022 prefers G or C as the bulged residue and, in the present study, the reason for this preference was analyzed by using RNAs with modified nucleoside residues as the bulged residue. It was found that the amino groups of bulged guanine and cytidine bases interact with the oxygen atoms of the backbone phosphate groups, and the oxygen and nitrogen atoms of bulged guanine and cytidine bases interact with the piperazine group of KG022. Thus, this work presents an example of the mechanism of the specific recognition of a small molecule by RNAs.

氟喹诺酮衍生物KG022与rna的相互作用:凸起残基的作用。
为了进一步推进rna结合小分子药物的发现,利用核磁共振光谱分析了单凸起rna与氟喹诺酮衍生物KG022之间的特异性相互作用。在我们之前的工作中,我们发现KG022位于凸起残基的3‘和5’侧的两个碱基对之间。KG022倾向于G或C作为凸起的残基,在本研究中,通过使用修饰核苷残基的rna作为凸起的残基来分析这种偏好的原因。结果表明,凸起的鸟嘌呤和胞苷基的氨基与主磷酸基的氧原子相互作用,凸起的鸟嘌呤和胞苷基的氧原子和氮原子与KG022的哌嗪基相互作用。因此,这项工作提出了rna特异性识别小分子机制的一个例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of biochemistry
Journal of biochemistry 生物-生化与分子生物学
CiteScore
4.80
自引率
3.70%
发文量
101
审稿时长
4-8 weeks
期刊介绍: The Journal of Biochemistry founded in 1922 publishes the results of original research in the fields of Biochemistry, Molecular Biology, Cell, and Biotechnology written in English in the form of Regular Papers or Rapid Communications. A Rapid Communication is not a preliminary note, but it is, though brief, a complete and final publication. The materials described in Rapid Communications should not be included in a later paper. The Journal also publishes short reviews (JB Review) and papers solicited by the Editorial Board.
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