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dc.contributor.authorCastillo, Jimmy-
dc.contributor.authorHung, Jeanette-
dc.contributor.authorRodríguez, María del C.-
dc.contributor.authorBastidas, Elsy-
dc.contributor.authorLaboren, Ivanna-
dc.contributor.authorJaimes, Alba-
dc.date.accessioned2017-01-19T16:39:06Z-
dc.date.available2017-01-19T16:39:06Z-
dc.date.issued2005-06-16-
dc.identifier.citationAnalytical Biochemistry 343 (2005) 293–298en_US
dc.identifier.issn0003-2697-
dc.identifier.urihttp://hdl.handle.net/10872/14054-
dc.description.abstractIn this work, we report an alternative assay for the determination of the inhibitory eVect on monoamine oxidase B (MAO-B) activity of probe compounds. Enzyme MAO-B exhibits Xuorescence emissions when it is excited at 412 nm. Using an inexpensive blue LED-like excitation source, we measured the quenching of Xuorescence intensity of MAO-B enzyme during the reaction with inhibitors. The applicability of the procedure is demonstrated by assays with L-deprenyl and berberine as inhibitors through the use of Xuorescence studies. The IC50 values of L-deprenyl and berberine were 0.04 and 90 M, respectively. The KI values were 0.020 and 47 M for L-deprenyl and berberine, respectively. These IC50 and KI values were similar to the values obtained with a standard method. These results demonstrate the feasibility of this method as an alternative to follow the inhibitory eVect on MAO-B.en_US
dc.language.isoen_USen_US
dc.publisherAnalytical Biochemistryen_US
dc.subjectMAO-Ben_US
dc.subjectLED FLUORESCENCEen_US
dc.subjectBERBERINEen_US
dc.titleLED Xuorescence spectroscopy for direct determination of monoamine oxidase B inactivationen_US
dc.typeArticleen_US
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