首页|多吡啶镍配合物的合成表征及与DNA和HSA的作用

多吡啶镍配合物的合成表征及与DNA和HSA的作用

Synthesis and Characterization of Polypyridine Nickel Complexes and Their Interaction with DNA and HSA

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合成了一种多吡啶单核镍金属配合物(Ni(acac)2(o-NPIP)](CH3OH)3),利用光谱和单晶衍射对镍配合物进行了表征,采用紫外吸收光谱、荧光猝灭光谱揭示镍配合物与DNA的结合方式,利用荧光光谱法研究镍配合物与人血清白蛋白(HSA)的猝灭机制、结合常数及作用方式.结果表明:镍配合物是六配位单核不对称的八面体结构,镍配合物以插入方式与DNA进行结合,结合常数Kb=1.17×104 L·mol-1.随着镍配合物加入,溴化乙啶(EB)-DNA的荧光强度呈现下降趋势,意味着镍配合物与EB之间进行了竞争,取代EB与DNA进行结合,表观键合常数Kapp=8.03×105 L·mol-1,镍配合物与DNA的键合能力中等.镍配合物以静态猝灭机理导致HSA的荧光猝灭,且镍配合物与HSA的结合常数Kb均为105数量级,表明有较强的结合能力.镍配合物与HSA的主要结合力为疏水作用力.同步荧光研究发现,色氨酸残基是镍配合物和HSA的结合点.因此,合成的新型多吡啶镍配合物与DNA的结合能力中等,且能够以较强的结合能力与HSA结合,具有较好的生物活性.
A polypyridine mononuclear nickel metal complex (Ni(acac)2(o-NPIP)](CH3OH)3) was synthesized,the nickel complexes were characterized by spectrum and single crystal diffraction.The binding mode of nickel complex and DNA was revealed by ultraviolet absorption spectrum and fluorescence quenching spectrum.The quenching mechanism,binding constant and action mode of nickel complex and HSA were studied by fluorescence spectroscopy.The results showed that the nickel complexes were six-coordinated mononuclear asymmetric octahedral structures.The nickel complex bonded to DNA by insertion,and the binding constant Kb=1.17×104 L·mol-1.With the addition of nickel complex,the fluorescence intensity of EB-DNA showed a decreasing trend,indicating that the nickel complex competed with EB to replace EB in binding DNA.The apparent bonding constant Kapp=8.03×105 L·mol-1,the nickel complex had moderate bonding DNA capacity.The fluorescence quenching of HSA was caused by the static quenching mechanism of nickel complex,and the binding constant Kb of nickel complex and HSA was 105 orders of magnitude,indicating a strong binding ability.The main binding force between nickel complexes and HSA was the hydrophobic force.Synchronous fluorescence study showed that tryptophan residue was the binding point of nickel complex and HSA.So,the new polypyridine nickel complex synthesized had moderate binding ability to DNA,and could bind to HSA with strong binding ability,and had good biological activity.

PolypyridineNickelComplexMolecular biologyUltraviolet spectrumFluorescence spectrumReactivity

赵晓飞、张培芳、曹冰雁、田炳欣、刘灿仿

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邢台医学高等专科学校第二附属医院临床药学科,河北邢台 054000

邢台医学高等专科学校第二附属医院门诊部,河北邢台 054000

邢台医学高等专科学校第二附属医院医务科,河北邢台 054000

邢台医学高等专科学校药学系,河北邢台 054000

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多吡啶 配合物 分子生物学 紫外光谱 荧光光谱 活性

河北省卫健委医学科研课题计划项目邢台市重点研发计划项目

202015932023ZC142

2024

当代化工
中国石油抚顺石化公司,中国石化抚顺石油化工研究院,沈阳市医药和化工行业联合会

当代化工

CSTPCD
影响因子:0.412
ISSN:1671-0460
年,卷(期):2024.53(9)
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