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六配位八面体络合物中孤立组氨酸与金属离子(镍、铜、锌)相互作用的密度泛函理论研究。

A DFT study of isolated histidine interactions with metal ions (Ni, Cu, Zn) in a six-coordinated octahedral complex.

作者信息

Franklin Latasha M, Walker Sharnek M, Hill Glake

机构信息

Department of Chemistry, Physics, and Atmospheric Sciences, Jackson State University, Jackson, MS, 39217, USA.

出版信息

J Mol Model. 2020 May 6;26(6):116. doi: 10.1007/s00894-020-04389-2.

Abstract

Understanding the role that metal ions play in biological and material processes is critical to addressing a number of diseases and problems facing society today. There have been a number of studies that have begun to approach this concern from a myriad of different perspectives. However, there is still a considerable lack of understanding concerning the mechanisms and structures of metal-related problems, specifically biological and medical-related issues. Understanding the mechanism of ingestion and uptake of metals into the human body is critical to addressing many diseases such as Alzheimer's and certain types of cancers. Using computational techniques, this work adds to the overall understanding of metal interactions with proteins by focusing on metal ion interactions with the amino acid, histidine, one of the most common sites of metal attachment. In this work, the geometries of single and dual histidines attached to Ni, Cu, and Zn ions at B3LYP/6-311G(d) are presented. The results show stable octahedral complexes associated with each of the metal ions. Free energy calculations suggest that all three complexes are spontaneous in the formation of the dual histidine-metal complexes. Nickel and copper are spontaneous in the formation of the single histidine complex, although the copper complex undergoes slight geometric changes. Zinc is found to be nonspontaneous in forming the single histidine complex. Finally, the reduction potential of the single histidine-metal complex is presented. All of the complexes show positive reduction potentials. However, the nickel and copper complexes undergo geometrical changes to adopt a square planar conformation. Graphical abstract The impact of metal ions in biological systems is of great importance to understanding a diverse number of diseases. By understanding the fundamentals of select ions complexed with histidines, greater understanding of the mechanisms of actions these ions play in health may be elucidated. This work presents initial structures and thermodynamics of histidine complexes with nickel, copper, and zinc metal ions.

摘要

了解金属离子在生物和材料过程中所起的作用对于解决当今社会面临的许多疾病和问题至关重要。已经有许多研究开始从无数不同的角度探讨这一问题。然而,对于与金属相关问题的机制和结构,特别是与生物和医学相关的问题,仍然存在相当大的认识不足。了解金属进入人体的摄取和吸收机制对于解决许多疾病,如阿尔茨海默病和某些类型的癌症至关重要。通过计算技术,这项工作通过关注金属离子与氨基酸组氨酸(金属附着的最常见位点之一)之间的相互作用,增加了对金属与蛋白质相互作用的整体理解。在这项工作中,展示了在B3LYP/6 - 311G(d)水平下与镍、铜和锌离子相连的单组氨酸和双组氨酸的几何结构。结果表明,每种金属离子都形成了稳定的八面体配合物。自由能计算表明,所有三种配合物在双组氨酸 - 金属配合物的形成过程中都是自发的。镍和铜在单组氨酸配合物的形成过程中是自发的,尽管铜配合物会发生轻微的几何变化。发现锌在形成单组氨酸配合物时是非自发的。最后,给出了单组氨酸 - 金属配合物的还原电位。所有配合物都显示出正的还原电位。然而,镍和铜配合物会发生几何变化以采用平面正方形构象。图形摘要 金属离子在生物系统中的影响对于理解多种疾病非常重要。通过了解与组氨酸络合的特定离子的基本原理,可以阐明这些离子在健康中所起作用的机制。这项工作展示了组氨酸与镍、铜和锌金属离子配合物的初始结构和热力学。

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