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dc.contributor.authorDvir, Tal
dc.contributor.authorBanghart, Matthew R.
dc.contributor.authorTimko, Brian P.
dc.contributor.authorLanger, Robert S
dc.contributor.authorKohane, Daniel S.
dc.date.accessioned2020-09-03T18:06:40Z
dc.date.available2020-09-03T18:06:40Z
dc.date.issued2009-11
dc.date.submitted2009-10
dc.identifier.issn1530-6984
dc.identifier.issn1530-6992
dc.identifier.urihttps://hdl.handle.net/1721.1/127167
dc.description.abstractWe report a novel and simple proof-of-concept of a nanoparticulate system that targets any tissue selectively upon illumination. Nanoparticles were covalently functionalized with the amino acid sequence YIGSR, which adheres to the β1 integrins present on most cell surfaces. This peptide was masked with a caging group, rendering it biologically inert. Illumination with UV light released the caging group from the YIGSR, allowing binding to cells.en_US
dc.description.sponsorshipNIH (Grant GM073626)
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/nl903411sen_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.titlePhoto-Targeted Nanoparticlesen_US
dc.typeArticleen_US
dc.identifier.citationDvir, Tal et al. "Photo-Targeted Nanoparticles." 10, 1 (January 2010): 250-254 © 2010 American Chemical Society
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalNano Letters
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.updated2019-09-03T18:43:00Z
dspace.date.submission2019-09-03T18:43:01Z
mit.metadata.statusComplete


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