Interaction between La3+ and MP-11 in the physiological solution

被引:13
作者
Guo, Shaofen
Zhou, Qing
Lu, Tianhong
Ding, Xiaolan
Huang, Xiaohua [1 ]
机构
[1] Nanjing Normal Univ, Coll Chem & Environm Sci, Nanjing 210097, Peoples R China
[2] So Yangtze Univ, Minist Educ, Key Lab Ind Biotechnol, Wuxi 214063, Peoples R China
[3] Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R China
[4] Tsing Hua Univ, Dept Biol Sci & Biotechnol, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
lanthanum; microperoxidase-11; interaction; electrochemical reaction;
D O I
10.1016/j.electacta.2006.08.023
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, the interaction between La3+ and microperoxidase-11 (MP-11) in the imitated physiological solution was investigated with the electrochemical method, circular dichroism (CD) and ultraviolet-visible (UV-vis) absorption spectroscopy. It was found that the interaction ways between La3+ and MP-11 are different with increasing the molar ratio of La3+ and MP-11. When the molar ratio of La3+ and MP-11 is less than 2, La3+ mainly interacts with the metacetonic acid group of the heme group in the MP-11 molecules, causing the increase in the non-planarity of the porphyrin cycle in the heme group and the decrease in the content of the random coil conformation of MP-11. These structural changes would increase the exposure extent of the electrochemical active center of MP-11 and thus, La3+ can promote the electrochemical reaction of MP-11 and its electrocatalytic activity for the reduction of H2O2 at the glassy carbon (GC) electrode. However, when the molar ratio of La3+ and MP-11 is larger than 3, except binding to the carbonyl oxygen of the metacetonic acid group in the heme group, La3+ interacts also with the oxygen-containing groups of the amides in the polypeptide chains of the MP-11 molecules, leading to the increase in the contents of the random coil conformation in the peptide of the MP-11 molecule, comparing with that for the molar ratio of less than 2. However, the non-planarity of the porphyrin cycle in the heme group is similar to that for the molar ratio of less than 2. Perhaps, the increase in the contents of the random coil conformation in the peptide of the MP-11 molecule would partially shield the electrochemical active center of MP-11 and is not favorable to the electrochemical and electrocatalytic reaction of MP-11. Thus, the reversibility, of the electrochemical reaction of MP-11 and its electrocatalytic activity for the reduction of H2O2 are lower than that for the molar ratio of less than 2. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2032 / 2038
页数:7
相关论文
共 62 条
[1]   INFLUENCES OF PI-PI-COMPLEX FORMATION, DIMERIZATION, AND BINDING TO HEMOGLOBIN ON THE PLANARITY OF NICKEL(II) PORPHYRINS [J].
ALDEN, RG ;
ONDRIAS, MR ;
SHELNUTT, JA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (02) :691-697
[2]   METAL-IONS AND COMPLEXES AS MODULATORS OF PROTEIN INTERFACIAL ELECTRON-TRANSPORT AT GRAPHITE-ELECTRODES [J].
ARMSTRONG, FA ;
COX, PA ;
HILL, HAO ;
LOWE, VJ ;
OLIVER, BN .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 217 (02) :331-366
[3]   PRION PROTEIN ISOFORMS, A CONVERGENCE OF BIOLOGICAL AND STRUCTURAL INVESTIGATIONS [J].
BALDWIN, MA ;
COHEN, FE ;
PRUSINER, SB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (33) :19197-19200
[4]   MOLECULAR-DYNAMICS STUDIES ON PEROXIDASES - A STRUCTURAL MODEL FOR HORSERADISH-PEROXIDASE AND A SUBSTRATE ADDUCT [J].
BANCI, L ;
CARLONI, P ;
SAVELLINI, GG .
BIOCHEMISTRY, 1994, 33 (41) :12356-12366
[5]   Control of cytochrome c redox potential:: Axial ligation and protein environment effects [J].
Battistuzzi, G ;
Borsari, M ;
Cowan, JA ;
Ranieri, A ;
Sola, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (19) :5315-5324
[6]   SPECTROSCOPIC STUDIES OF METAL-ION BINDING TO A TRYPTOPHAN-CONTAINING PARVALBUMIN [J].
BREEN, PJ ;
HILD, EK ;
HORROCKS, WD .
BIOCHEMISTRY, 1985, 24 (19) :4991-4997
[7]   MEMBRANE-ENTRAPPED MICROPEROXIDASE AS A SOLID-STATE PROMOTER IN THE ELECTROCHEMISTRY OF SOLUBLE METALLOPROTEINS [J].
BRUNORI, M ;
SANTUCCI, R ;
CAMPANELLA, L ;
TRANCHIDA, G .
BIOCHEMICAL JOURNAL, 1989, 264 (01) :301-304
[8]   CIRCULAR DICHROIC ANALYSIS OF PROTEIN CONFORMATION - INCLUSION OF BETA-TURNS [J].
CHANG, CT ;
WU, CSC ;
YANG, JT .
ANALYTICAL BIOCHEMISTRY, 1978, 91 (01) :13-31
[9]   Structural and conformational stability of horseradish peroxidase: Effect of temperature and pH [J].
Chattopadhyay, K ;
Mazumdar, S .
BIOCHEMISTRY, 2000, 39 (01) :263-270
[10]   Lanthanide ions induce hydrolysis of hemoglobin-bound 2,3-diphosphoglycerate (2,3-DPG), conformational changes of globin and bidirectional changes of 2,3-DPG-hemoglobin's oxygen affinity [J].
Cheng, Y ;
Lin, HK ;
Xue, DP ;
Li, RC ;
Wang, K .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2001, 1535 (02) :200-216