Neurotransmitters and neural hormone-based probes for quadruplex DNA sequences associated with neurodegenerative diseases.

IF 1.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleosides, Nucleotides & Nucleic Acids Pub Date : 2024-11-19 DOI:10.1080/15257770.2024.2431145
Callie Rohrer, Alexis Palumbo, Marissa Paul, Erin Reese, Swarna Basu
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Abstract

The potential of neurotransmitters and neural hormones as possible G-quadruplex DNA binders was analyzed using fluorescence spectroscopy, surface-enhanced Raman spectroscopy (SERS), DNA melting analysis, and molecular docking. G-quadruplex sequences, (GGC)3 and G4C2, with roles in Fragile X syndrome and amyotrophic lateral sclerosis (ALS), respectively, were selected, and their interactions with melatonin, serotonin, and gamma-aminobutyric acid (GABA), were studied. Both melatonin and serotonin demonstrated strong interactions with the DNA sequences with hydrogen bonding being the primary mode of interaction, with some non-intercalative interactions involving the π systems. GABA demonstrated much weaker interactions and may not be a suitable candidate as a probe for low concentrations of G-quadruplex DNA.

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基于神经递质和神经激素的探针,用于检测与神经退行性疾病相关的四重 DNA 序列。
利用荧光光谱学、表面增强拉曼光谱(SERS)、DNA熔融分析和分子对接分析了神经递质和神经激素作为可能的G-四叠体DNA结合剂的潜力。研究人员选择了分别在脆性 X 综合征和肌萎缩性脊髓侧索硬化症(ALS)中发挥作用的 G-四叠体序列 (GGC)3 和 G4C2,并研究了它们与褪黑激素、血清素和γ-氨基丁酸(GABA)的相互作用。褪黑激素和血清素都与 DNA 序列发生了强烈的相互作用,氢键是主要的相互作用模式,其中一些非交变相互作用涉及到 π 系统。GABA 的相互作用要弱得多,可能不适合作为低浓度 G 型四联 DNA 的探针。
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来源期刊
Nucleosides, Nucleotides & Nucleic Acids
Nucleosides, Nucleotides & Nucleic Acids 生物-生化与分子生物学
CiteScore
2.60
自引率
7.70%
发文量
91
审稿时长
6 months
期刊介绍: Nucleosides, Nucleotides & Nucleic Acids publishes research articles, short notices, and concise, critical reviews of related topics that focus on the chemistry and biology of nucleosides, nucleotides, and nucleic acids. Complete with experimental details, this all-inclusive journal emphasizes the synthesis, biological activities, new and improved synthetic methods, and significant observations related to new compounds.
期刊最新文献
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