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dc.creatorVasić, Vesna M.
dc.creatorJovanovic, D
dc.creatorHorvat, Anica
dc.creatorMomić, Tatjana
dc.creatorNizezic, G
dc.date.accessioned2018-03-01T19:04:12Z
dc.date.available2018-03-01T19:04:12Z
dc.date.issued2002
dc.identifier.issn0003-2697
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2496
dc.description.abstractIn the present study a polystyrene microtiter plate was tested as a support material for synaptic plasma membrane (SPM) immobilization by adsorption. The adsorption was carried out by an 18-h incubation at +4degreesC of SPM with a polystyrene matrix, at pH 7.4. Evaluation of the efficiency of the applied immobilization method revealed that 10% protein fraction of initially applied SPM was bound to the support and that two SPM enzymes, Na+/K+-ATPase and Mg2+-ATPase, retained 70-80% activity after the adsorption. In addition, adsorption stabilizes Na+/K+-ATPase and Mg2+-ATPase, since the activities are substantial 3 weeks after the adsorption. Parallel kinetic analysis showed that adsorption does not alter significantly the kinetic properties of Na+/K+-ATPase and Mg2+-ATPase and their sensitivity to and mechanism of Cd2+- or Hg2+- induced inhibition. The only exception is the high affinity Mg2+-ATPase moiety, whose affinity for ATP and sensitivity toward Cd2+ were increased by the adsorption. The results show that such system may be used as a practical and comfortable model for the in vitro toxicological investigations. (C) 2001 Elsevier Science.en
dc.rightsrestrictedAccessen
dc.sourceAnalytical Biochemistryen
dc.subjectNa+/K+-ATPaseen
dc.subjectMg2+-ATPaseen
dc.subjectsynaptic plasma membranesen
dc.subjectAdsorptionen
dc.subjectheavy metalsen
dc.subjectkineticsen
dc.titleEffect of Cd2+ and Hg2+ on the activity of Na+/K+-ATPase and Mg2+-ATPase adsorbed on polystyrene microtiter platesen
dc.typearticleen
dcterms.abstractНизезиц, Г; Јовановиц, Д; Васић Весна М; Хорват, Aница; Момић Татјана;
dc.citation.volume300
dc.citation.issue2
dc.citation.spage113
dc.citation.epage120
dc.identifier.wos000173371000002
dc.identifier.doi10.1006/abio.2001.5405
dc.citation.rankM21
dc.identifier.pmid11779101
dc.identifier.scopus2-s2.0-0037080992


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