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dc.contributor.authorSu, Xingfang
dc.contributor.authorYang, Nicole Jie Yeon
dc.contributor.authorWittrup, Karl Dane
dc.contributor.authorIrvine, Darrell J
dc.date.accessioned2013-08-02T17:23:07Z
dc.date.available2013-08-02T17:23:07Z
dc.date.issued2013-04
dc.date.submitted2013-02
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602
dc.identifier.urihttp://hdl.handle.net/1721.1/79767
dc.description.abstractPlant-derived Type I toxins are candidate anticancer therapeutics requiring cytosolic delivery into tumor cells. We tested a concept for two-stage delivery, whereby tumor cells precoated with an antibody-targeted gelonin toxin were killed by exposure to endosome-disrupting polymer nanoparticles. Co-internalization of particles and tumor cell-bound gelonin led to cytosolic delivery and >50-fold enhancement of toxin efficacy. This approach allows the extreme potency of gelonin to be focused on tumors with significantly reduced potential for off-target toxicity.en_US
dc.description.sponsorshipUnited States. Dept. of Defense (Institute for Soldier Nanotechnology, contract W911NF-07-D-0004)en_US
dc.description.sponsorshipHoward Hughes Medical Institute (Investigator)en_US
dc.description.sponsorshipSingapore. Agency for Science, Technology and Researchen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/bm3019906en_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.titleSynergistic Antitumor Activity from Two-Stage Delivery of Targeted Toxins and Endosome-Disrupting Nanoparticlesen_US
dc.typeArticleen_US
dc.identifier.citationSu, Xingfang, Nicole Yang, K. Dane Wittrup, and Darrell J. Irvine. Synergistic Antitumor Activity from Two-Stage Delivery of Targeted Toxins and Endosome-Disrupting Nanoparticles. Biomacromolecules 14, no. 4 (April 8, 2013): 1093-1102.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.departmentRagon Institute of MGH, MIT and Harvarden_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorSu, Xingfangen_US
dc.contributor.mitauthorYang, Nicole Jie Yeonen_US
dc.contributor.mitauthorWittrup, Karl Daneen_US
dc.contributor.mitauthorIrvine, Darrell J.en_US
dc.relation.journalBiomacromoleculesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSu, Xingfang; Yang, Nicole; Wittrup, K. Dane; Irvine, Darrell J.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2398-5896
dc.identifier.orcidhttps://orcid.org/0000-0002-0882-7761
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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