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dc.contributor.authorAllen, M
dc.contributor.authorBulte, J. W. M.
dc.contributor.authorLiepold, L.
dc.contributor.authorBasu, Gautam
dc.contributor.authorZywicke, H. A.
dc.contributor.authorFrank, J. A.
dc.contributor.authorYoung, M.
dc.contributor.authorDouglas, T.
dc.date.accessioned2013-03-26T09:41:39Z
dc.date.available2013-03-26T09:41:39Z
dc.date.issued2005-10
dc.identifierFOR ACCESS / DOWNLOAD PROBLEM -- PLEASE CONTACT LIBRARIAN, BOSE INSTITUTE, akc@bic.boseinst.ernet.inen_US
dc.identifier.citationAllen M. Bulte JW, Liepold L. B~su G. Zywicke HA, Frank lA. Young M. *DougJas T. "Paramagnetic vIral nanoparticles as potential high-relaxivity magnetic resonance contrast agents" Magn Reson Med. 54. 807 -812 (2005i.en_US
dc.identifier.issn0740-3194
dc.identifier.uri1.Full Text Link ->
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/mrm.20614/pdfen_US
dc.identifier.uri=================================================en_US
dc.identifier.uri2.Scopus : Citation Link ->en_US
dc.identifier.urihttp://www.scopus.com/record/display.url?eid=2-s2.0-26844517318&origin=resultslist&sort=plf-f&src=s&st1=Paramagnetic+vIral+nanoparticles+as+potential+high-relaxivity+magnetic+resonance+contrast+agents&sid=6843A8EDB7A028EAB388F064B7281F3E.mw4ft95QGjz1tIFG9A1uw%3a20&sot=b&sdt=b&sl=111&s=TITLE-ABS-KEY%28Paramagnetic+vIral+nanoparticles+as+potential+high-relaxivity+magnetic+resonance+contrast+agents%29&relpos=0&relpos=0&searchTerm=TITLE-ABS-KEY%28Paramagnetic+vIral+nanoparticles+as+potential+high-relaxivity+magnetic+resonance+contrast+agents%29en_US
dc.descriptionDOI: 10.1002/mrm.20614en_US
dc.description.abstractIn order to compensate for the inherent high threshold of detectability of MR contrast agents, there has been an active interest in the development of paramagnetic nanoparticles incorporating high payloads of Gd3+ with high molecular relaxivities. Toward this end, the protein cage of Cowpea chlorotic mottle virus (CCMV), having 180 metal binding sites, is being explored. In vivo CCMV binds Ca2+ at specific metal binding sites; however, Gd3+ can also bind at these sites. Using fluorescence resonance energy transfer we have characterized the binding affinity of Gd3+ to the metal binding sites by competition experiments with Tb3+. The measured dissociation constant (K-d) for Gd3+ bound to the virus is 31 mu M. The T-1 and T-2 relaxivities of solvent water protons in the presence of Gd3+-bound CCMV were 202 and 376 mM(-1) s(-1), respectively, at 61 MHz Larmor frequency. The unusually high relaxivity values of the Gd3+-CCMV are largely a result of the nanoparticle virus size and the large number of Gd3+ ions bound to the virus. These preliminary results should encourage further investigations into the use of viral protein cages as a new platform for MR contrast agents.en_US
dc.language.isoenen_US
dc.publisherJOHN WILEYen_US
dc.subjectvirus particlesen_US
dc.subjectFRETen_US
dc.subjectMR contrast agenten_US
dc.subjectrelaxometryen_US
dc.subjectgadoliniumen_US
dc.subjectANR-2005-06en_US
dc.subjectWOS:000232348000008en_US
dc.titleParamagnetic viral nanoparticles as potential high-relaxivity magnetic resonance contrast agentsen_US
dc.title.alternativeMAGNETIC RESONANCE IN MEDICINEen_US
dc.typeArticleen_US


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