Structural characterization and reactivity of γ-octamolybdate functionalized by proline

被引:53
作者
Cartuyvels, Els [1 ]
Van Hecke, Kristof [1 ]
Van Meervelt, Luc [1 ]
Gorller-Walrand, Christiane [1 ]
Parac-Vogt, Tatjana N. [1 ]
机构
[1] Katholieke Univ Leuven, Dept Chem, B-3001 Louvain, Belgium
关键词
octamolybdate; proline; ATP hydrolysis; P-31; NMR; Mo-95;
D O I
10.1016/j.jinorgbio.2008.02.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The reaction of molybdate and DL-proline at pH 3.4 results in the formation of a Na-4[Mo8O26(proO)(2)]center dot 22H(2)O Complex (pro = proline) in which two proline ligands are attached to molybdenum(VI) ions via monodentate coordination of the carboxylate groups. The structure of the complex was determined by single crystal X-ray diffraction and by combination of H-1, C-13 and Mo-95 NMR spectroscopy techniques in solution. The structure of the complex is strongly dependant on the pH. At native pH 3.4 the octamolybdate-type structure seems to be present in solution, but the increase of pH to 5.8 resulted in a rearrangement of the structure to a heptamolybdate-type structure. At physiological pH, the polyoxometalate framework was completely dissociated into the monomeric MoO42- unit. The reactivity of the Na-4[Mo8O26(proO)(2)]center dot 22H(2)O towards the hydrolysis of ATP was tested at different pH values. While in solution at pH 3.4 the hydrolysis proceeded to yield AMP (adenosine monophosphate) and ADP (adenosine diphosphate) in nearly equal amounts, reaction mixture at pH 5.8 gave ADP as the only product of hydrolysis after 24 h of reaction. At neutral pH, the hydrolysis of ATP was slower, but it proceeded to yield 75% of ADP after 48 h of reaction. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1589 / 1598
页数:10
相关论文
共 38 条
[1]  
*BRUK AN XRAY SYST, 1997, SAINT MAN VERS 5 6 0, P84102
[2]  
*BRUK AN XRAY SYST, 1997, SHELXTL NT MAN VERS
[3]   Questioning the paradigm of metal complex promoted phosphodiester hydrolysis:: [Mo7O24]6- polyoxometalate cluster as an unlikely catalyst for the hydrolysis of a DNA model substrate [J].
Cartuyvels, Els ;
Absillis, Gregory ;
Parac-Vogt, Tatjana N. .
CHEMICAL COMMUNICATIONS, 2008, (01) :85-87
[4]   Structural and antitumor activity study of γ-octamolybdates containing aminoacids and peptides [J].
Cindric, M ;
Novak, TK ;
Kraljevic, S ;
Kralj, M ;
Kamenar, B .
INORGANICA CHIMICA ACTA, 2006, 359 (05) :1673-1680
[5]   Synthesis and structure of K2[HMo6(VI)V(V)O22(NH3CH2COO)3]•8H2O:: a new example of a polyoxomolybdovanadate coordinated by a glycinato ligand [J].
Cindric, M ;
Strukan, N ;
Devcic, M ;
Kamenar, B .
INORGANIC CHEMISTRY COMMUNICATIONS, 1999, 2 (11) :558-560
[6]  
Cruywagen JJ, 2000, ADV INORG CHEM, V49, P127
[7]   Mechanism of the protective effect of heteropolyoxotungstate against herpes simplex virus type 2 [J].
Dan, K ;
Miyashita, K ;
Seto, Y ;
Fujita, H ;
Yamase, T .
PHARMACOLOGY, 2003, 67 (02) :83-89
[8]   ANTITUMOR-ACTIVITY OF NEW ANTITUMOR SUBSTANCE, POLYOXOMOLYBDATE, AGAINST SEVERAL HUMAN CANCERS IN ATHYMIC NUDE-MICE [J].
FUJITA, H ;
FUJITA, T ;
SAKURAI, T ;
YAMASE, T ;
SETO, Y .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 168 (02) :421-426
[9]   H-1 AND P-31 NMR-STUDY OF THE INTERACTION OF MOLYBDATE WITH THE NUCLEOTIDES ADENOSINE 5'-DIPHOSPHATE AND ADENOSINE 5'-TRIPHOSPHATE [J].
GERALDES, CFGC ;
CASTRO, MMCA .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1986, 28 (2-3) :319-327
[10]   Cytotoxic effects of novel polyoxotungstates and a platinum compound on human cancer cell lines [J].
Gerth, HUV ;
Rompel, A ;
Krebs, B ;
Boos, J ;
Lanvers-Kaminsky, C .
ANTI-CANCER DRUGS, 2005, 16 (01) :101-106