洞察 G 型四联 DNA 的相互作用:阴离子 Zn(II) 和 Co(II) 酞菁-四磺酸盐配合物的对比分析。

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Recognition Pub Date : 2024-03-12 DOI:10.1002/jmr.3082
Efkan Bağda
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引用次数: 0

摘要

G 型四联体在调节基因表达和复制等各种细胞过程中发挥着关键作用,因此成为了解和操纵细胞功能的重要结构。G 型四叠体配体的开发为治疗和研究应用带来了巨大前景,提供了有针对性的工具来调节 G 型四叠体结构,并有可能影响关键的生物通路。G- 四叉研究的一个令人兴奋的前沿领域是探索阴离子配体及其对稳定和调节 G- 四叉 DNA 的深远影响。在本研究中,研究了两种阴离子酞菁化合物(锌(II)酞菁 3,4',4″,4‴-四磺酸四钠盐,ZnAPC;钴(II)酞菁 3,4',4″,4‴-四磺酸四钠盐,CoAPC)与三个独立的 G-四链形成 DNA 序列的相互作用。相互作用是通过 DNA 聚合酶停止研究和光谱研究进行的。根据实验数据的结果,可以确定 ZnAPC 与 G 型四联 DNA 结构发生了积极的相互作用。另一方面,人们认为 ZnAPC 与 CoAPC 的相互作用较小,甚至只是简单的静电作用。计算了与 ZnAPC 相互作用的 KD 常数和 Bmax 常数。发现 AS1411、Vegf 和 Tel21 与 ZnAPC 的 KD 常数分别为 (1.16 ± 0.07) × 10-5 、 (9.75 ± .24) × 10-6 和 (1.00 ± 0.36) × 10-4 M。因此,结论是 ZnAPC 能与 G 型四链 DNA 配体有效地相互作用。
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Insights into the G-quadruplex DNA interaction landscape: Comparative analysis of anionic Zn(II) and Co(II) phthalocyanine-tetrasulfonate complexes

G-quadruplexes play a pivotal role in regulating various cellular processes, including gene expression and replication, making them essential structures in understanding, and manipulating cellular functions. The development of G-quadruplex ligands holds significant promise in therapeutic and research applications, offering targeted tools to modulate G-quadruplex structures and potentially influence critical biological pathways. An exciting frontier in G-quadruplex research lies in the exploration of anionic ligands, and their profound impact on stabilizing and modulating G-quadruplex DNA. In this study, the interaction of two anionic phthalocyanine compounds (Zinc (II) phthalocyanine 3,4′,4″,4‴-tetrasulfonic acid, tetrasodium salt, ZnAPC; cobalt (II) phthalocyanine 3,4′,4″,4‴-tetrasulfonic acid, tetrasodium salt, CoAPC) and three separate G-quadruplex-forming DNA sequences was investigated. Interactions were carried out by DNA polymerase stop studies along with spectroscopic studies. According to the results of experimental data, it was determined that ZnAPC actively interacts with the G-quadruplex DNA structures. On the other hand, it was thought that the interaction with CoAPC was less and even occurred in simple electrostatic interactions. KD constants and Bmax constants for the interaction with ZnAPC were calculated. The KD constants for ZnAPC were found to be (1.16 ± 0.07) × 10−5, (9.75 ± .24) × 10−6 and (1.00 ± 0.36) × 10−4 M for AS1411, Vegf, and Tel21, respectively. Accordingly, it was concluded that ZnAPC interacts with G-quadruplex DNA ligands effectively.

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来源期刊
Journal of Molecular Recognition
Journal of Molecular Recognition 生物-生化与分子生物学
CiteScore
4.60
自引率
3.70%
发文量
68
审稿时长
2.7 months
期刊介绍: Journal of Molecular Recognition (JMR) publishes original research papers and reviews describing substantial advances in our understanding of molecular recognition phenomena in life sciences, covering all aspects from biochemistry, molecular biology, medicine, and biophysics. The research may employ experimental, theoretical and/or computational approaches. The focus of the journal is on recognition phenomena involving biomolecules and their biological / biochemical partners rather than on the recognition of metal ions or inorganic compounds. Molecular recognition involves non-covalent specific interactions between two or more biological molecules, molecular aggregates, cellular modules or organelles, as exemplified by receptor-ligand, antigen-antibody, nucleic acid-protein, sugar-lectin, to mention just a few of the possible interactions. The journal invites manuscripts that aim to achieve a complete description of molecular recognition mechanisms between well-characterized biomolecules in terms of structure, dynamics and biological activity. Such studies may help the future development of new drugs and vaccines, although the experimental testing of new drugs and vaccines falls outside the scope of the journal. Manuscripts that describe the application of standard approaches and techniques to design or model new molecular entities or to describe interactions between biomolecules, but do not provide new insights into molecular recognition processes will not be considered. Similarly, manuscripts involving biomolecules uncharacterized at the sequence level (e.g. calf thymus DNA) will not be considered.
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