Forero-Girón Angie Carolay, Toro-Labbé Alejandro
Laboratorio de Química Teórica Computacional (QTC), Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Avenida Vicuña Mackenna 4860, 7820436, Santiago de Chile, Chile.
J Mol Model. 2025 Jan 3;31(1):32. doi: 10.1007/s00894-024-06256-w.
Dopamine -monooxygenase (D 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 M, forming a hydroperoxo intermediate and dopamine radical. It was found that the formation of a hydrogen bond between dopamine and the D 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.
The dopamine and a computational model of the copper superoxo complex on D 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.
多巴胺单加氧酶(D-M)是生物体中的一种关键酶,它能区域选择性地将多巴胺转化为R-去甲肾上腺素。本文所研究反应的关键步骤是一个氢原子从多巴胺转移至D-M上的超氧配合物,形成氢过氧中间体和多巴胺自由基。研究发现,多巴胺与D-M催化剂之间形成氢键会增强底物与酶的相互作用,并促进氢原子转移选择性地发生,从而生成所需对映体形式的产物。为了确定最可能的反应机制,使用理论和计算工具详细分析了导致氢过氧中间体形成的六个反应。反应力分析已被用于证明活化能的性质主要是结构性的,并且很大程度上是由于物种的初始接近,以便彼此更靠近以促进氢的提取。另一方面,反应电子流表明驱动反应的电子活性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中,它以协同且非自发的方式发生。已经确定了驱动反应的化学事件,并详细量化了每个事件吸收或释放的能量。
在Gaussian 16软件包中,采用B3LYP-D3(BJ)/6-311G(d,p)理论水平对多巴胺和D-M上铜超氧配合物的计算模型进行了优化。在气相中并通过PCM溶剂化模型进行优化和内禀反应坐标(IRC)计算,以模拟蛋白质介质。使用NCI-plot软件绘制非共价相互作用。