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pubmed-article:14751267pubmed:dateCreated2004-1-30lld:pubmed
pubmed-article:14751267pubmed:abstractTextCaspases are a group of cysteine proteases involved in apoptosis and inflammation. A multiparametric homogeneous assay capable of measuring activity of three different caspases in a single well of a microtiter plate is described. Different fluorescent europium, samarium, terbium, and dysprosium chelates were coupled to a caspase substrate peptide, their luminescence properties, were analyzed, and their function in a time-resolved fluorescence quenching-based caspase 3 assay was studied. Substrates for caspases 1, 2, 3, 6, and 8 and granzyme B were also synthesized and their specificities for different caspases were determined. By selecting suitable lanthanide chelates and substrates we developed a multiparametric homogeneous time-resolved fluorescence quenching-based assay for caspases 1, 3, and 6. The assay was capable of measuring the activity of both single caspases and a mixture of three caspases mixed in the same well.lld:pubmed
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pubmed-article:14751267pubmed:authorpubmed-author:HakalaHarriHlld:pubmed
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pubmed-article:14751267pubmed:pagination317-25lld:pubmed
pubmed-article:14751267pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:14751267pubmed:year2004lld:pubmed
pubmed-article:14751267pubmed:articleTitleCaspase multiplexing: simultaneous homogeneous time-resolved quenching assay (TruPoint) for caspases 1, 3, and 6.lld:pubmed
pubmed-article:14751267pubmed:affiliationPerkinElmer Life and Analytical Sciences, Wallac Oy, P.O. Box 10, FIN-20101, Turku, Finland. jarkko.karvinen@perkinelmer.comlld:pubmed
pubmed-article:14751267pubmed:publicationTypeJournal Articlelld:pubmed