Synthesis, crystal structures, molecular docking and in vitro cytotoxicity studies of two new copper(II) complexes: special emphasis on their binding to HSA

作者：Shen, Fang; Liu, Ya-Xian; Li, Shu-Min; Jiang, Chi-Kun; Wang, Bing-Feng; Xiong, Ya-Hong^*; Mao, Zong-Wan; Le, Xue-Yi^*

来源：New Journal of Chemistry, 2017, 41(21): 12429-12441.

DOI：10.1039/c7nj02351k

• HUMAN-SERUM-ALBUMIN
• DNA-BINDING
• ANTICANCER ACTIVITY
• ANTITUMOR AGENTS
• METAL-COMPLEXES
• DRUG
• DERIVATIVES
• ANTIBACTERIAL
• CLEAVAGE
• PROTEIN

Two new mixed-ligand copper(II) complexes, [Cu(PyTA)(L-Phe)Cl]center dot 2H(2)O (1), [Cu(PyTA)(L-Met)Cl]center dot 0.5H(2)O (2) (where PyTA = 2,4-diamino-6-(2'-pyridyl)-1,3,5-triazine, L-Phe = L-phenylalanine, L-Met = L-methionine), were synthesized and characterized by elemental analysis, IR, UV-vis, molar conductivity, ESI-MS, and X-ray crystal diffraction. The copper centers of complexes 1 and 2 are in slightly distorted square pyramidal environments, and fluorescence quenching experiments and calorimetry showed that the complexes bound to human serum albumin (HSA) with high affinities (binding constants K-D = 3.71 x 10(6) L mol(-1) for 1 and 1.99 x 10(6) L mol(-1) for 2, 1 > 2). UV-vis and circular dichroism (CD) spectroscopic investigations revealed that the complexes induced the alteration of hydrophobic environments and the decrease in the a-helix level of HSA during binding processes. Synchronous fluorescence spectra demonstrated that the binding sites of the complexes on HSA were close to the Trp-214 residue in the IIA subdomain, which was further verified by site marker competitive experiments and the molecular docking method. In vitro cytotoxicity experiments showed that the effective HSA-binding interactions enhanced the cytotoxicity of the complexes. Both 1 and 2 displayed strong anticancer activities against the Eca-109 cell line and induced cell death through the apoptosis pathway.

• 单位
  华南热带农业大学; 华南农业大学; 中山大学