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dc.contributor.authorPluth, Michael D.
dc.contributor.authorChan, Maria R.
dc.contributor.authorMcQuade, Lindsey E.
dc.contributor.authorLippard, Stephen J.
dc.date.accessioned2012-10-18T14:29:21Z
dc.date.available2012-10-18T14:29:21Z
dc.date.issued2011-09
dc.date.submitted2011-05
dc.identifier.issn0020-1669
dc.identifier.issn1520-510X
dc.identifier.urihttp://hdl.handle.net/1721.1/74070
dc.description.abstractFluorescent turn-on probes for nitric oxide based on seminaphthofluorescein scaffolds were prepared and spectroscopically characterized. The Cu(II) complexes of these fluorescent probes react with NO under anaerobic conditions to yield a 20–45-fold increase in integrated emission. The seminaphthofluorescein-based probes emit at longer wavelengths than the parent FL1 and FL2 fluorescein-based generations of NO probes, maintaining emission maxima between 550 and 625 nm. The emission profiles depend on the excitation wavelength; maximum fluorescence turn-on is achieved at excitations between 535 and 575 nm. The probes are highly selective for NO over other biologically relevant reactive nitrogen and oxygen species including NO3–, NO2–, HNO, ONOO–, NO2, OCl–, and H2O2. The seminaphthofluorescein-based probes can be used to visualize endogenously produced NO in live cells, as demonstrated using Raw 264.7 macrophages.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CHE-0611944)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (K99GM092970)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ic200986ven_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Lippard via Erja Kajosaloen_US
dc.titleSeminaphthofluorescein-Based Fluorescent Probes for Imaging Nitric Oxide in Live Cellsen_US
dc.typeArticleen_US
dc.identifier.citationPluth, Michael D. et al. “Seminaphthofluorescein-Based Fluorescent Probes for Imaging Nitric Oxide in Live Cells.” Inorganic Chemistry 50.19 (2011): 9385–9392.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverLippard, Stephen J.
dc.contributor.mitauthorPluth, Michael D.
dc.contributor.mitauthorChan, Maria R.
dc.contributor.mitauthorMcQuade, Lindsey E.
dc.contributor.mitauthorLippard, Stephen J.
dc.relation.journalInorganic Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPluth, Michael D.; Chan, Maria R.; McQuade, Lindsey E.; Lippard, Stephen J.en
dc.identifier.orcidhttps://orcid.org/0000-0002-2693-4982
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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