Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2254
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dc.contributor.authorDhamija, S.-
dc.contributor.authorThakur, Bhisham-
dc.contributor.authorGuptasarma, P.-
dc.contributor.authorDe, A.K.-
dc.date.accessioned2020-11-26T06:19:52Z-
dc.date.available2020-11-26T06:19:52Z-
dc.date.issued2018-
dc.identifier.citationFaraday Discussions, 207, pp. 39-54en_US
dc.identifier.otherhttps://doi.org/10.1039/C7FD00187H-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/fd/c7fd00187h#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2254-
dc.description.abstractFluorescent proteins exhibit interesting excited state photochemistry, leading to bright fluorescence emission that renders their versatile biological role and wide use as biomarkers. A molecular-level mechanism of the excited state dynamics is desirable to pinpoint the origin of the bright fluorescence of these proteins. Here we present studies on a yellow fluorescent protein variant, Venus, and investigate the photophysics behind the dual fluorescence emission upon UV excitation. Based on our studies, we propose that the unique nature of the potential energy surface is responsible for the observation of minor fluorescence in Venus which is not seen in wild type GFP.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectGreen Fluorescent Proteinsen_US
dc.subjectfluorescent proteinsen_US
dc.subjectQuantum Theoryen_US
dc.titleProbing the excited state dynamics of Venus: origin of dual-emission in fluorescent proteinsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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