Inhibitory effect of platinum and ruthenium bipyridyl complexes on porcine pancreatic phospholipase A2

被引:7
|
作者
Kamceva, Tina [1 ]
Flemmig, Joerg [2 ]
Damnjanovic, Bojana [1 ]
Arnhold, Juergen [2 ]
Mijatovic, Aleksandar [3 ]
Petkovic, Marijana [1 ]
机构
[1] Univ Belgrade, Inst Nucl Sci Vinca, Phys Chem Lab, Belgrade, Serbia
[2] Univ Leipzig, Fac Med, Inst Med Phys & Biophys, D-04107 Leipzig, Germany
[3] Univ Kragujevac, Fac Sci, Dept Chem, Kragujevac 34000, Serbia
关键词
ASSISTED LASER-DESORPTION; FLIGHT MASS-SPECTROMETRY; MALDI-TOF MS; BINDING-SITE; ANTICANCER DRUGS; INSULINOMA CELLS; CYCLOSPORINE-A; CANCER-CELLS; IONIZATION; CISPLATIN;
D O I
10.1039/c1mt00088h
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
Pancreatic phospholipase A(2) (PLA(2)) plays an important role in cellular homeostasis as well as in the process of carcinogenesis. Effects of metallo-drugs used as chemotherapeutics on the activity of this enzyme are unknown. In this work, the interaction between porcine pancreatic PLA(2) and two selected transition metal complexes-tetrachloro(bipyridine) platinum(IV) ([PtCl4(bipy)]) and dichloro (bipyridine) ruthenium(III)chloride ([RuCl2(bipy)(2)]Cl)-was studied. Matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) and fluorescence spectroscopy have been used to analyse the enzyme activity in the absence and presence of metal complexes and to verify potential binding of these drugs to the enzyme. The tested metal complexes decreased the activity of phospholipase A(2) in an uncompetitive inhibition mode. A binding of the ruthenium complex near the active site of the enzyme could be evidenced and possible modes of interaction are discussed.
引用
收藏
页码:1056 / 1063
页数:8
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