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dc.contributor.authorLiu, Pei-Hanen_US
dc.contributor.authorUrban, Pawel L.en_US
dc.date.accessioned2018-08-21T05:53:01Z-
dc.date.available2018-08-21T05:53:01Z-
dc.date.issued2017-12-15en_US
dc.identifier.issn0003-2697en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ab.2017.10.007en_US
dc.identifier.urihttp://hdl.handle.net/11536/144184-
dc.description.abstractThe temporal effects of luciferase reaction luminescence have only been discussed in the context of light intensity (flash vs. glow). However, alterations in the color of the light emitted over the course of the luciferase reaction have not been reported. Here, we show a temporal change in the light color emitted during the reaction catalyzed by unmodified firefly luciferase when concentrations of one of the substrates, adenosine triphosphate (ATP), are gradually increased. The temporal color change from green to red occurs within the first few minutes of the luciferase reaction when an ATP-containing solution is either added or synthesized in situ with the aid of an autocatalytic reaction occurring simultaneously. This color change is not accompanied by pH changes. An analysis of the red and green channels demonstrates dissimilar kinetics, suggesting the co-existence of two or more temporally shifted luminescence pathways. The implications of these findings might improve dual-color biosensing/imaging protocols and influence the engineering of biophotonic systems.en_US
dc.language.isoen_USen_US
dc.subjectATP assayen_US
dc.subjectColor switchingen_US
dc.subjectLuciferaseen_US
dc.subjectLuminescenceen_US
dc.titleSpontaneous luminescence color change in the firefly luciferase assay systemen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ab.2017.10.007en_US
dc.identifier.journalANALYTICAL BIOCHEMISTRYen_US
dc.citation.volume539en_US
dc.citation.spage54en_US
dc.citation.epage59en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000417117000010en_US
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