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以DPA-Bpy为五齿配体的Fe(II)配合物的光谱学、结构、生物大分子相互作用及抗增殖活性

Spectroscopy, Structure, Biomacromolecular Interactions, and Antiproliferation Activity of a Fe(II) Complex With DPA-Bpy as Pentadentate Ligand.

作者信息

Bai Hehe, Shi Jia, Guo Qingyu, Wang Wenming, Zhang Zhigang, Li Yafeng, Vennampalli Manohar, Zhao Xuan, Wang Hongfei

机构信息

Key Laboratory of Chemical Biology and Molecular Engineering of the Education Ministry, Institute of Molecular Science, Shanxi University, Taiyuan, China.

The Fifth Hospital (Shanxi Provincial People's Hospital) of Shanxi Medical University, Taiyuan, China.

出版信息

Front Chem. 2022 Apr 25;10:888693. doi: 10.3389/fchem.2022.888693. eCollection 2022.

Abstract

An Fe(II) complex with DPA-Bpy (DPA-Bpy = N,N-bis(2-pyridinylmethyl)-2,20-bipyridine-6 -methanamine) as the ligand was synthesized and characterized to mimic bleomycin. The binding constants ( ) of the complex with calf thymus DNA and human serum albumin (HSA) were quantitatively evaluated using fluorescence spectroscopy, with as 5.53×10 and 2.40×10 M, respectively; the number of the average binding site () is close to 1. The thermodynamic analyses suggested that the electrostatic interactions exist between the complex and DNA, and the hydrogen bonding and Van der Waals force exist for the complex and HSA. The Fe complex exhibits cleavage ability toward pBR322 DNA, and the crystal structure of the HSA Fe complex adduct at 2.4 Å resolution clearly shows that His288 serves as the axial ligand of the Fe center complexed with a pentadentate DPA-Bpy ligand. Furthermore, the cytotoxicity of the complex was evaluated against HeLa cells. Both the Fe complex and HSA Fe complex adduct show obvious effect on cell proliferation with an IC of 1.18 and 0.82 μM, respectively; they induced cell apoptosis and arrested cell cycles at S phase. This study provides insight into the plausible mechanism underlying their metabolism and pharmacological activity.

摘要

合成并表征了一种以DPA-Bpy(DPA-Bpy = N,N-双(2-吡啶基甲基)-2,2'-联吡啶-6-甲胺)为配体的Fe(II)配合物,以模拟博来霉素。利用荧光光谱法定量评估了该配合物与小牛胸腺DNA和人血清白蛋白(HSA)的结合常数( ),分别为5.53×10 和2.40×10 M;平均结合位点数量( )接近1。热力学分析表明,该配合物与DNA之间存在静电相互作用,与HSA之间存在氢键和范德华力。Fe配合物对pBR322 DNA具有切割能力,分辨率为2.4 Å的HSA Fe配合物加合物的晶体结构清楚地表明,His288作为与五齿DPA-Bpy配体络合的Fe中心的轴向配体。此外,评估了该配合物对HeLa细胞的细胞毒性。Fe配合物和HSA Fe配合物加合物对细胞增殖均有明显影响,IC 分别为1.18和0.82 μM;它们诱导细胞凋亡并使细胞周期停滞在S期。本研究为其代谢和药理活性的潜在机制提供了深入见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/9081768/9b25445989b8/fchem-10-888693-g010.jpg

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