NMDA 受体与芬太尼、氯胺酮和异氟醚相互作用的结构洞察:揭示结合模式的计算研究。

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Atif Khalid, Nabeela Farhat
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引用次数: 0

摘要

如果 NMDA 受体在临床相关浓度下受到药物调节,那么它们就会被认为是许多麻醉剂的靶点。异氟醚和氯胺酮等挥发性麻醉剂与 NMDA 受体相互作用,抑制通道活化,从而在临床相关浓度下阻断 NMDA 神经传递。人们对氯胺酮、异氟烷和芬太尼等常用药物的结合模式知之甚少。我们利用分子对接、分子动力学模拟和 DFT 计算这些药物与 NMDA 受体的结合。利用定义明确的计算方法,我们发现这些药物具有较高的对接得分,并与受体有显著的相互作用。这些药物与底物结合口袋结合,形成了大量的相互作用。我们发现这些相互作用是稳定的,并且具有较低的 HOMO-LUMO 能隙。这项研究为药物与 NMDA 受体之间强烈而稳定的相互作用提供了足够的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structural Insight on Interaction of NMDA receptor with fentanyl, ketamine and Isoflurane: A Computational Study to Unravel Mode of Binding.

Structural Insight on Interaction of NMDA receptor with fentanyl, ketamine and Isoflurane: A Computational Study to Unravel Mode of Binding.

NMDA receptors are considered targets for many anesthetics if they are modulated by the drugs at clinically relevant concentrations. Volatile anesthetics like isoflurane and ketamine interact with NMDA receptors, inhibiting channel activation and thus blocking NMDA neurotransmission at clinically relevant concentrations. The mode of binding of commonly used drugs like ketamine, isoflurane, and fentanyl is poorly understood. We used molecular docking, molecular dynamics simulations, and DFT calculation of these drugs against the NMDA receptor. Using well-defined computational methods, we identified that these drugs have high docking scores and significant interaction with receptors. These drugs bind to the substrate-binding pocket and form a remarkable number of interactions. We have found that these interactions are stable and have low HOMO-LUMO energy gaps. This study provides enough evidences of strong and stable interaction between drugs and NMDA receptor.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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