Show simple item record

dc.contributor.authorLangford, Troy F.
dc.contributor.authorHuang, Beijing Kara
dc.contributor.authorLim, Joseph B.
dc.contributor.authorMoon, Sun Jin
dc.contributor.authorSikes Johnson, Hadley
dc.date.accessioned2019-03-07T15:08:40Z
dc.date.available2019-03-07T15:08:40Z
dc.date.issued2018-08
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/120784
dc.description.abstractRedox cancer therapeutics target the increased reliance on intracellular antioxidant systems and enhanced susceptibility to oxidant-induced stress of some cancer cells compared to normal cells. Many of these therapeutics are thought to perturb intracellular levels of the oxidant hydrogen peroxide (H[subscript 2]O[subscript 2]), a signaling molecule that modulates a number of different processes in human cells. However, fluorescent probes for this species remain limited in their ability to detect the small perturbations induced during successful treatments. We report a fluorescent sensor based upon human peroxiredoxin-2, which acts as the natural indicator of small H[subscript 2]O[subscript 2] fluctuations in human cells. The new probe reveals peroxide-induced oxidation in human cells below the detection limit of current probes, as well as peroxiredoxin-2 oxidation caused by two different redox cancer therapeutics in living cells. This capability will be useful in elucidating the mechanism of current redox-based therapeutics and in developing new ones.en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipSamsung Fellowshipen_US
dc.description.sponsorshipMassachusetts Institute of Technology (Haas Family Fellowship in Chemical Engineering)en_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41467-018-05557-yen_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleMonitoring the action of redox-directed cancer therapeutics using a human peroxiredoxin-2-based probeen_US
dc.typeArticleen_US
dc.identifier.citationLangford, Troy F., Beijing K. Huang, Joseph B. Lim, Sun Jin Moon, and Hadley D. Sikes. “Monitoring the Action of Redox-Directed Cancer Therapeutics Using a Human Peroxiredoxin-2-Based Probe.” Nature Communications 9, no. 1 (August 7, 2018). © 2018 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorLangford, Troy F.
dc.contributor.mitauthorHuang, Beijing Kara
dc.contributor.mitauthorLim, Joseph B.
dc.contributor.mitauthorMoon, Sun Jin
dc.contributor.mitauthorSikes Johnson, Hadley
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-03-04T14:47:05Z
dspace.orderedauthorsLangford, Troy F.; Huang, Beijing K.; Lim, Joseph B.; Moon, Sun Jin; Sikes, Hadley D.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6003-681X
dc.identifier.orcidhttps://orcid.org/0000-0002-9238-8932
dc.identifier.orcidhttps://orcid.org/0000-0002-7096-138X
mit.licensePUBLISHER_CCen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record