寻找一种可光开关的血清素受体药物:一项分子动力学模拟研究

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-06-23 DOI:10.1039/D5RA03789A
Arshjot S. Dhaliwal, Arunima Verma and Padmabati Mondal
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引用次数: 0

摘要

g蛋白偶联受体是一种膜结合蛋白,控制人体的生理和心理活动,如激素调节、感觉信号和神经传递。偶氮苯的光异构化能力使新一代可光转换药物的开发成为可能,这些药物在减少常规治疗典型副作用的同时提供更大的疗效。5 -羟色胺与5 -羟色胺受体的结合可以通过偶氮苯在羟基位置的顺式和反式光开关异构体偶联来控制。我们结合分子动力学(MD)模拟和自由能方法研究了受体与反式偶氮苯融合5 -羟色胺(TAS)和顺式偶氮苯融合5 -羟色胺(CAS)配体系统的结合。与TAS配体相比,CAS配体经历了更大的构象波动。结合自由能值在CAS -受体和TAS -受体复合物之间存在显著差异,表明TAS配体比CAS配体更能与5 -羟色胺受体结合。它还揭示了脂质膜的存在对受体-配体复合物的稳定性和动力学有很强的影响,从而对差分结合自由能值也有很大的影响。cas -受体和tas -受体复合物之间结合自由能的变化是由熵驱动的。对感兴趣的芳香残基与每个配体之间的堆叠相互作用进行定性和定量分析表明,t型堆叠相互作用占主导地位,特别是Trp327和Phe330残基对tas -受体复合物的稳定性有显著贡献。该研究表明,利用偶氮苯的光开关特性,可以设计一种具有可调结合亲和力的光开关色氨酸药物,这可能有助于精神健康治疗的先进药物发现和治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In search of a photoswitchable drug for serotonin receptors: a molecular dynamics simulation study†

In search of a photoswitchable drug for serotonin receptors: a molecular dynamics simulation study†

G-protein-coupled receptors are membrane-bound proteins that control physiological and psychological activities such as hormonal regulation, sensory signaling and neurotransmission in the human body. The photoisomerization capability of azobenzenes has enabled the development of a new generation of photoswitchable drugs that offer greater efficacy while reducing the side effects typical of conventional treatments. Serotonin binding to the serotonin receptor can be controlled by conjugating it with cis and trans photoswitchable isomers of azobenzene at the hydroxyl position. We have used a combination of molecular dynamics (MD) simulation and free-energy methods for receptor binding to trans-azobenzene-fused-serotonin (TAS) and cis-azobenzene-fused serotonin (CAS) ligand systems. The CAS ligand experienced greater conformational fluctuations in comparison to the TAS ligand. Binding free-energy values showed significant differences between the CAS–receptor and TAS–receptor complexes, indicating that the TAS ligand binds actively to the serotonin receptor as compared to the CAS ligand. It also revealed that the presence of a lipid membrane has a strong influence on the stability and dynamics of the receptor–ligand complex and, thus, on the differential binding free-energy values. The change in binding free energy between the CAS–receptor and TAS–receptor complexes is found to be entropically driven. A qualitative and quantitative analysis of the stacking interactions between aromatic residues of interest and each ligand indicates that T-type stacking interactions predominate and particularly Trp327 and Phe330 residues contribute notably to the stability of the TAS–receptor complex. The study indicates that by leveraging the photoswitchable properties of azobenzenes, a photoswitchable serotonin-based drug with tunable binding affinity can be designed, which may facilitate advanced drug discovery and therapeutic approaches for mental health treatments.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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