How does dopamine convert into norepinephrine? Insights on the key step of the reaction

IF 2.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Modeling Pub Date : 2025-01-03 DOI:10.1007/s00894-024-06256-w
Angie Carolay Forero-Girón, Alejandro Toro-Labbé
{"title":"How does dopamine convert into norepinephrine? Insights on the key step of the reaction","authors":"Angie Carolay Forero-Girón,&nbsp;Alejandro Toro-Labbé","doi":"10.1007/s00894-024-06256-w","DOIUrl":null,"url":null,"abstract":"<div><h3>Context</h3><p>Dopamine <span>\\(\\beta \\)</span>-monooxygenase (D<span>\\(\\beta \\)</span>M) is an essential enzyme in the organism that regioselectively converts dopamine into R-norepinephrine, the key step of the reaction, studied in this paper, is a hydrogen atom transfer (HAT) from dopamine to a superoxo complex on D<span>\\(\\beta \\)</span>M, forming a hydroperoxo intermediate and dopamine radical. It was found that the formation of a hydrogen bond between dopamine and the D<span>\\(\\beta \\)</span>M catalyst strengthens the substrate-enzyme interaction and facilitates the HAT which takes place selectively to give the desired enantiomeric form of the product. Six reactions leading to the hydroperoxo intermediate were analyzed in detail using theoretical and computational tools in order to identify the most probable reaction mechanism. The reaction force analysis has been used to demonstrate that the nature of the activation energy is mostly structural and largely due to the initial approach of species in order to get closer to each other to facilitate the hydrogen abstraction. On the other hand, the reaction electronic flux revealed that electronic activity driving the reactions is triggered by polarization effects and, in the most probable reaction among the six studied, it takes place in a concerted and non-spontaneous way. Chemical events driving the reaction have been identified and the energy absorbed or delivered by each one was quantified in detail.</p><h3>Methods</h3><p>The dopamine and a computational model of the copper superoxo complex on D<span>\\(\\beta \\)</span>M were optimized at B3LYP-D3(BJ)/6-311 G(d,p) level theory in the Gaussian 16 software package. Optimization and IRC calculations were performed in the gas phase and through the PCM solvation model to mimic the protein medium. Non-covalent interactions were plotted using the NCI-plot software.</p><h3>Graphical abstract</h3><p>The interaction of dopamine with copper superoxo complex on D<span>\\(\\beta \\)</span>M is studied in order to characterize the mechanism of the hydrogen atom transfer step in the conversion of dopamine into norepinephrine.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":651,"journal":{"name":"Journal of Molecular Modeling","volume":"31 1","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Modeling","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00894-024-06256-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Context

Dopamine \(\beta \)-monooxygenase (D\(\beta \)M) is an essential enzyme in the organism that regioselectively converts dopamine into R-norepinephrine, the key step of the reaction, studied in this paper, is a hydrogen atom transfer (HAT) from dopamine to a superoxo complex on D\(\beta \)M, forming a hydroperoxo intermediate and dopamine radical. It was found that the formation of a hydrogen bond between dopamine and the D\(\beta \)M catalyst strengthens the substrate-enzyme interaction and facilitates the HAT which takes place selectively to give the desired enantiomeric form of the product. Six reactions leading to the hydroperoxo intermediate were analyzed in detail using theoretical and computational tools in order to identify the most probable reaction mechanism. The reaction force analysis has been used to demonstrate that the nature of the activation energy is mostly structural and largely due to the initial approach of species in order to get closer to each other to facilitate the hydrogen abstraction. On the other hand, the reaction electronic flux revealed that electronic activity driving the reactions is triggered by polarization effects and, in the most probable reaction among the six studied, it takes place in a concerted and non-spontaneous way. Chemical events driving the reaction have been identified and the energy absorbed or delivered by each one was quantified in detail.

Methods

The dopamine and a computational model of the copper superoxo complex on D\(\beta \)M were optimized at B3LYP-D3(BJ)/6-311 G(d,p) level theory in the Gaussian 16 software package. Optimization and IRC calculations were performed in the gas phase and through the PCM solvation model to mimic the protein medium. Non-covalent interactions were plotted using the NCI-plot software.

Graphical abstract

The interaction of dopamine with copper superoxo complex on D\(\beta \)M is studied in order to characterize the mechanism of the hydrogen atom transfer step in the conversion of dopamine into norepinephrine.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
多巴胺如何转化为去甲肾上腺素?洞察反应的关键步骤
多巴胺\(\beta \) -单加氧酶(dopamine -monooxygenase, D \(\beta \) M)是生物体内区域选择性地将多巴胺转化为r -去甲肾上腺素的必需酶,本文研究的关键步骤是多巴胺的氢原子转移(HAT)到D \(\beta \) M上的超氧复合物上,形成氢过氧中间体和多巴胺自由基。研究发现,多巴胺和D \(\beta \) M催化剂之间氢键的形成加强了底物-酶的相互作用,促进了HAT的选择性发生,从而得到所需的产物对映体形式。为了确定最可能的反应机理,利用理论和计算工具对六个生成氢过氧中间体的反应进行了详细的分析。反作用力分析表明,活化能的性质主要是结构性的,很大程度上是由于物种的初始接近,以便彼此接近,以促进氢的提取。另一方面,反应的电子通量揭示了驱动反应的电子活动是由极化效应触发的,并且在所研究的六个反应中,最可能的反应是以协调和非自发的方式发生的。驱动反应的化学事件已被确定,每个事件所吸收或传递的能量也被详细地量化了。方法利用Gaussian 16软件包中的B3LYP-D3(BJ)/6-311 G(D,p)水平理论,对D \(\beta \) M上的多巴胺和铜超氧配合物的计算模型进行优化。优化和IRC计算在气相进行,并通过PCM溶剂化模型模拟蛋白质介质。非共价相互作用用NCI-plot软件绘制。图摘要研究了多巴胺与D \(\beta \) M上铜超氧配合物的相互作用,以表征多巴胺转化为去甲肾上腺素的氢原子转移步骤的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Molecular Modeling
Journal of Molecular Modeling 化学-化学综合
CiteScore
3.50
自引率
4.50%
发文量
362
审稿时长
2.9 months
期刊介绍: The Journal of Molecular Modeling focuses on "hardcore" modeling, publishing high-quality research and reports. Founded in 1995 as a purely electronic journal, it has adapted its format to include a full-color print edition, and adjusted its aims and scope fit the fast-changing field of molecular modeling, with a particular focus on three-dimensional modeling. Today, the journal covers all aspects of molecular modeling including life science modeling; materials modeling; new methods; and computational chemistry. Topics include computer-aided molecular design; rational drug design, de novo ligand design, receptor modeling and docking; cheminformatics, data analysis, visualization and mining; computational medicinal chemistry; homology modeling; simulation of peptides, DNA and other biopolymers; quantitative structure-activity relationships (QSAR) and ADME-modeling; modeling of biological reaction mechanisms; and combined experimental and computational studies in which calculations play a major role.
期刊最新文献
First-principles studies of the SCl2 adsorption on the doped boron phosphide monolayer Investigation of product formation in the H + H2C = C = CH reaction: a comparison of experimental and theoretical kinetics The effect of pressure on the mechanical properties of hydroxyl-terminated polybutadiene-based propellants Structure and dynamics of anacardic acid in hexane, ethanol, and carbon tetrachloride: a molecular dynamics investigation Exploring the explosive potential of 2,3-dihydrofuran derivatives as novel insensitive high-energy density materials
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1