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dc.contributor.authorChen, Fangyi
dc.contributor.authorTang, Qi
dc.contributor.authorBian, Ke
dc.contributor.authorHumulock, Zachary T.
dc.contributor.authorYang, Xuedong
dc.contributor.authorLi, Deyu
dc.contributor.authorJost, Marco
dc.contributor.authorDrennan, Catherine L.
dc.contributor.authorEssigmann, John M.
dc.date.accessioned2018-06-19T13:15:21Z
dc.date.available2018-06-19T13:15:21Z
dc.date.issued2016-02
dc.date.submitted2015-12
dc.identifier.issn0893-228X
dc.identifier.issn1520-5010
dc.identifier.urihttp://hdl.handle.net/1721.1/116395
dc.description.abstractThe AlkB protein is a repair enzyme that uses an α-ketoglutarate/Fe(II)-dependent mechanism to repair alkyl DNA adducts. AlkB has been reported to repair highly susceptible substrates, such as 1-methyladenine and 3-methylcytosine, more efficiently in ss-DNA than in ds-DNA. Here, we tested the repair of weaker AlkB substrates 1-methylguanine and 3-methylthymine and found that AlkB prefers to repair them in ds-DNA. We also discovered that AlkB and its human homologues, ABH2 and ABH3, are able to repair the aforementioned adducts when the adduct is present in a mismatched base pair. These observations demonstrate the strong adaptability of AlkB toward repairing various adducts in different environments. (Chemical Equation Presented).en_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ACS.CHEMRESTOX.5B00522en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleAdaptive Response Enzyme AlkB Preferentially Repairs 1-Methylguanine and 3-Methylthymine Adducts in Double-Stranded DNAen_US
dc.typeArticleen_US
dc.identifier.citationChen, Fangyi et al. “Adaptive Response Enzyme AlkB Preferentially Repairs 1-Methylguanine and 3-Methylthymine Adducts in Double-Stranded DNA.” Chemical Research in Toxicology 29, 4 (March 2016): 687–693 © 2016 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Environmental Health Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorJost, Marco
dc.contributor.mitauthorDrennan, Catherine L.
dc.contributor.mitauthorEssigmann, John M
dc.relation.journalChemical Research in Toxicologyen_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
dc.date.updated2018-06-15T17:18:07Z
dspace.orderedauthorsChen, Fangyi; Tang, Qi; Bian, Ke; Humulock, Zachary T.; Yang, Xuedong; Jost, Marco; Drennan, Catherine L.; Essigmann, John M.; Li, Deyuen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2196-5691
mit.licensePUBLISHER_POLICYen_US


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