Warshel Institute for Computational Biology, School of Life and Health Sciences, The Chinese University of Hong Kong, Shenzhen, Longgang District, 518172, Shenzhen, P. R. China.
Chem Asian J. 2022 Jul 1;17(13):e202200360. doi: 10.1002/asia.202200360. Epub 2022 May 24.
Drug compounds or their metabolic intermediates (MIs) sometimes inhibit the function of cytochrome P450 enzymes (P450s) by forming a coordination bond with the Fe(III) heme or Fe(II) heme of P450s. Such inhibition is one of the major causes of drug-drug interactions (DDIs), a subject of longstanding academic and practical interest. However, such coordination bonding is not fully understood at the quantum mechanical level, thus hampering rational improvement of the accuracy of DDI-related predictions. In this work, we employed density functional theory (DFT) and the generalized Kohn-Sham energy decomposition analysis (GKS-EDA) scheme to investigate the nature of the coordination bonding formed in the reversible and quasi-irreversible inhibition of P450s. The GKS-EDA results highlighted a previously unrecognized role of the electron correlation effect in P450 inhibition. The correlation effect tends to be larger in Fe(II) complexes of MI-type inhibitors and is particularly prominent for the nitrosoalkane ligand. An additional natural bond orbital (NBO) analysis provided insight into the relative significance of the σ donation and π backdonation effects in various heme-inhibitor complexes.
药物化合物或其代谢中间体 (MIs) 有时通过与 P450 酶的 Fe(III) 血红素或 Fe(II) 血红素形成配位键来抑制细胞色素 P450 酶 (P450s) 的功能。这种抑制是药物相互作用 (DDI) 的主要原因之一,这是一个长期以来备受学术界和实践界关注的课题。然而,这种配位键在量子力学水平上还不完全清楚,从而阻碍了提高与 DDI 相关预测准确性的合理性。在这项工作中,我们采用了密度泛函理论 (DFT) 和广义 Kohn-Sham 能量分解分析 (GKS-EDA) 方案来研究可逆和准不可逆抑制 P450s 时形成的配位键的性质。GKS-EDA 结果突出了电子相关效应在 P450 抑制中的先前未被认识到的作用。相关效应在 MI 型抑制剂的 Fe(II) 配合物中较大,对于亚硝基烷烃配体尤其明显。额外的自然键轨道 (NBO) 分析提供了对各种血红素抑制剂配合物中 σ 供体和 π 反馈效应相对重要性的深入了解。