Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9946
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dc.rights.licenserestrictedAccess-
dc.contributor.authorKameva T.-
dc.contributor.authorFlemmig J.-
dc.contributor.authorDamnjanovic B.-
dc.contributor.authorArnhold J.-
dc.contributor.authorMijatović, Aleksandar-
dc.contributor.authorPetkovic, Marijana-
dc.date.accessioned2021-04-20T14:28:19Z-
dc.date.available2021-04-20T14:28:19Z-
dc.date.issued2011-
dc.identifier.issn1756-5901-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9946-
dc.description.abstractPancreatic 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) ([PtCl 4(bipy)]) and dichloro (bipyridine) ruthenium(iii)chloride ([RuCl 2(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. © 2011 The Royal Society of Chemistry.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceMetallomics-
dc.titleInhibitory effect of platinum and ruthenium bipyridyl complexes on porcine pancreatic phospholipase A <inf>2</inf>-
dc.typearticle-
dc.identifier.doi10.1039/c1mt00088h-
dc.identifier.scopus2-s2.0-80053607258-
Appears in Collections:Faculty of Science, Kragujevac

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