高等学校化学学报 ›› 2009, Vol. 30 ›› Issue (11): 2154.

• 研究论文 • 上一篇    下一篇

钙调素与重金属Pb2+结合反应的方波极谱与循环伏安法研究

刘德龙1, 吴彦环1, 郭慧芳2, 白娟2, 孙大业2   

  1. 1. 河北师范大学化学学院,
    2. 生命科学学院, 石家庄 050016
  • 收稿日期:2009-05-31 出版日期:2009-11-10 发布日期:2009-11-10
  • 通讯作者: 刘德龙, 男, 博士, 教授, 主要从事生物分析化学与化学生物学方面研究. E-mail: delongliu9012@sina.com
  • 基金资助:

    国家自然科学基金(批准号: 20475013)资助.

Direct Binding of Reaction Pb2+ to Calmodulin by Square Wave Polarography and Cyclic Voltametry

LIU De-Long1*, WU Yan-Huan1, GUO Hui-Fang2, BAI Juan2, SUN Da-Ye2   

  1. 1. College of Chemistry,
    2. College of Life Science, Hebei Normal University, Shijiazhuang 050016, China
  • Received:2009-05-31 Online:2009-11-10 Published:2009-11-10
  • Contact: LIU De-Long. E-mail: delongliu9012@sina.com
  • Supported by:

    国家自然科学基金(批准号: 20475013)资助.

摘要:

采用方波极谱法研究了重金属Pb2+与钙调素(CaM)的结合反应, 直接检测到Pb2+-CaM配合物的存在, 并进一步利用循环伏安法研究了Pb2+-CaM的电极反应. 在pH=6.5时, 用方波极谱法在Pb2+-CaM体系中检测出2个还原峰, 峰电位分别为-0.44~-0.47 V和-0.73~-0.77 V, 说明在Pb2+-CaM体系中铅有2种存在形式, -0.44~-0.47 V的还原峰对应于游离态Pb2+, 电位更负的还原峰对应于配合物[Pb2+-CaM]. 2个还原峰的峰电流均随着cPb2+/cCaM比值增大而增大; 至cPb2+/cCaM≥10后, 配合物[Pb2+-CaM]的峰电流基本不再变化, 而游离态Pb2+的峰电流则继续增大. 利用极谱滴定曲线的拐点可判断出Pb2+在CaM中有10个结合位点. 进一步的测量结果表明, 循环伏安曲线出现游离态Pb2+的氧化峰和还原峰, 而络合态的[Pb2+-CaM]只有其还原峰, 反向电压扫描时不出现阳极波, 即没有相对应的氧化峰出现.

关键词: 钙调素; 重金属离子Pb2+; 结合位点; 方波极谱法; 循环伏安法

Abstract:

Calmodulin(CaM) is a highly conserved Ca2+ binding protein ubiquitously found in animals and plants, which is involved in a large variety of cellular functions. The presence of many other metal ions in the physiological and nonphysiological environment such as heavy metal ions suggests that CaM might be binding other metal ions than Ca2+, which might influnce CaM′s function. It is important to investigate the general metal ion binding properties of CaM. Based on high sensitivity of square wave polarographic signal of Pb2+, the direct binding reaction of Pb2+ to CaM was studied by square wave polarography(SWP). The complexing specie, Pb2+-CaM, was detected for the first time by SWP in the Pb2+-CaM system, and electrochemical reaction characterization was done by cyclic voltammetry. Two reduction peaks were detected in SWP polarograms obtained at different concentration ratios of Pb2+ to CaM at pH=6.5, indicating that two electroactive species of Pb2+ exist, the reduction peak potentials of two species are in the range of -0.44—-0.47 V and -0.73—-0.77 V vs. SCE, respectively. The peak with a maximum at ca. -0.44—-0.47 V is corresponding to the reduction of free Pb2+ under our experimental conditions and the peak with a maximum at ca. -0.73—-0.77 V, clearly more negative than that for the reduction of free Pb2+, allows us to interpret it as due to the reduction of Pb2+ complexed by CaM. Moreover, prior to the addition 10 times of Pb2+, two peak currents increase gradually with the increasing of the Pb2+ concentration. At higher metal ion concentration(10—16 times), the peak currents of free Pb2+ increased linearly with a higher value of the slope, while the peak currents of the complexing specie, Pb2+-CaM, reached maximal and constant. The polarographic titration curves of the two species show that there are ten binding sites in CaM at pH=6.5. Furthermore, the reduction species of Pb2+-CaM system was confirmed by cyclic voltammetry with Controlled Growth Mercury Electrode(CGME). One couple of the free Pb2+ redox waves were observed clearly in the cyclic voltammogram, and only the reduction peak of the complexing specie of Pb2+-CaM system was detected. The results obtained in the paper show a direct evidence for the mechanism of the toxicity of Pb2+ by CaM mediating.

Key words: Calmodulin; Heavy metal ion Pb2+; Binding site; Square wave polarography; Cyclic voltammetry

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