Department of Biochemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.
Department of Chemistry, Isfahan University of Technology, Isfahan, Iran.
J Mol Model. 2021 Jan 17;27(2):40. doi: 10.1007/s00894-020-04631-x.
O6-methylguanine DNA methyl transferase (MGMT) is a metalloenzyme participating in the repair of alkylated DNA. In this research, we performed a comparative study for evaluating the impact of zinc metal ion on the behavior and interactions of MGMT in the both enzymatic forms of apo MGMT and holo MGMT. DNA and proliferating cell nuclear antigen (PCNA), as partners of MGMT, were utilized to evaluate molecular interactions by virtual microscopy of molecular dynamics simulation. The stability and conformational alterations of each forms (apo and holo) MGMT-PCNA, and (apo and holo) MGMT-DNA complexes were calculated by MM/PBSA method. A total of seven systems including apo MGMT, holo MGMT, free PCNA, apo MGMT-PCNA, holo MGMT-PCNA, apo MGMT-DNA, and holo MGMT-DNA complexes were simulated. In this study, we found that holo MGMT was more stable and had better folding and functional properties than that of apo MGMT. Simulation analysis of (apo and holo) MGMT-PCNA complexes displayed that the sequences of the amino acids involved in the interactions were different in the two forms of MGMT. The important amino acids of holo MGMT involved in its interaction with PCNA included E92, K101, A119, G122, N123, P124, and K125, whereas the important amino acids of apo MGMT included R128, R135, S152, N157, Y158, and L162. Virtual microscopy of molecular dynamics simulation showed that the R128 and its surrounding residues were important amino acids involved in the interaction of holo MGMT with DNA that was exactly consistent with X-ray crystallography structure. In the apo form of the protein, the N157 and its surrounding residues were important amino acids involved in the interaction with DNA. The binding free energies of - 387.976, - 396.226, - 622.227, and - 617.333 kcal/mol were obtained for holo MGMT-PCNA, apo MGMT-PCNA, holo MGMT-DNA, and apo MGMT-DNA complexes, respectively. The principle result of this research was that the area of molecular interactions differed between the two states of MGMT. Therefore, in investigations of metalloproteins, the metal ion must be preserved in their structures. Finally, it is recommended to use the holo form of metalloproteins in in vitro and in silico researches.
O6-甲基鸟嘌呤 DNA 甲基转移酶 (MGMT) 是一种参与烷基化 DNA 修复的金属酶。在这项研究中,我们进行了一项比较研究,以评估锌金属离子对无蛋白 MGMT 和全蛋白 MGMT 两种酶形式中 MGMT 行为和相互作用的影响。DNA 和增殖细胞核抗原 (PCNA) 作为 MGMT 的伴侣,被用于通过虚拟显微镜分子动力学模拟来评估分子相互作用。通过 MM/PBSA 方法计算每个形式 (apo 和 holo) MGMT-PCNA 和 (apo 和 holo) MGMT-DNA 复合物的稳定性和构象变化。总共模拟了七个系统,包括 apo MGMT、holo MGMT、游离 PCNA、apo MGMT-PCNA、holo MGMT-PCNA、apo MGMT-DNA 和 holo MGMT-DNA 复合物。在这项研究中,我们发现 holo MGMT 比 apo MGMT 更稳定,折叠和功能特性更好。(apo 和 holo) MGMT-PCNA 复合物的模拟分析显示,两种形式的 MGMT 中参与相互作用的氨基酸序列不同。holo MGMT 与 PCNA 相互作用的重要氨基酸包括 E92、K101、A119、G122、N123、P124 和 K125,而 apo MGMT 的重要氨基酸包括 R128、R135、S152、N157、Y158 和 L162。分子动力学模拟的虚拟显微镜显示,R128 及其周围残基是 holo MGMT 与 DNA 相互作用的重要氨基酸,这与 X 射线晶体结构完全一致。在蛋白质的 apo 形式中,N157 及其周围残基是与 DNA 相互作用的重要氨基酸。得到了 holo MGMT-PCNA、apo MGMT-PCNA、holo MGMT-DNA 和 apo MGMT-DNA 复合物的结合自由能分别为-387.976、-396.226、-622.227 和-617.333 kcal/mol。这项研究的主要结果是 MGMT 的两种状态之间的分子相互作用区域不同。因此,在研究金属蛋白酶时,必须将金属离子保存在其结构中。最后,建议在体外和计算机模拟研究中使用金属蛋白酶的全蛋白形式。