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dc.contributor.authorMin, Kyoung Ah  Concept link
dc.contributor.authorRajeswaran, Walajapet G.  Concept link
dc.contributor.authorOldenbourg, Rudolf  Concept link
dc.contributor.authorHarris, Grant  Concept link
dc.contributor.authorKeswani, Rahul K.  Concept link
dc.contributor.authorChiang, Mason  Concept link
dc.contributor.authorRzeczycki, Phillip  Concept link
dc.contributor.authorTalattof, Arjang  Concept link
dc.contributor.authorHafeez, Mahwish  Concept link
dc.contributor.authorHorobin, Richard W.  Concept link
dc.contributor.authorLarsen, Scott D.  Concept link
dc.contributor.authorStringer, Kathleen A.  Concept link
dc.contributor.authorRosania, Gus R.  Concept link
dc.date.accessioned2015-09-22T18:04:36Z
dc.date.available2015-09-22T18:04:36Z
dc.date.issued2015-06-05
dc.identifier.citationAdvanced Science 2 (2015): 1500025en_US
dc.identifier.urihttps://hdl.handle.net/1912/7540
dc.description© The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Advanced Science 2 (2015): 1500025, doi:10.1002/advs.201500025.en_US
dc.description.abstractClofazimine is an orally administered drug that massively bioaccumulates in macrophages, forming membrane-bound intracellular structures possessing nanoscale supramolecular features. Here, a library of phenazine compounds derived from clofazimine is synthesized and tested for ability to accumulate and form ordered molecular aggregates inside cells. Regardless of chemical structure or physicochemical properties, bioaccumulation is consistently greater in macrophages than in epithelial cells. Microscopically, some self-assembled structures exhibit a pronounced, diattenuation anisotropy signal, evident by the differential absorption of linearly polarized light, at the peak absorbance wavelength of the phenazine core. The measured anisotropy is well above the background anisotropy of endogenous cellular components, reflecting the self-assembly of condensed, insoluble complexes of ordered phenazine molecules. Chemical variations introduced at the R-imino position of the phenazine core lead to idiosyncratic effects on the compounds' bioaccumulation behavior as well as on the morphology and organization of the resulting intracellular structures. Beyond clofazimine, these results demonstrate how the self-assembly of membrane permeant, orally bioavailable small molecule building blocks can endow cells with unnatural structural elements possessing chemical, physical, and functional characteristics unlike those of other natural cellular components.en_US
dc.description.sponsorshipThe authors acknowledge financial support from NIH (Grant R01GM078200 to G.R.R. and R01EB002583 to R.O.), a Rackham Predoctoral Fellowship Award to K.A.M., and University of Michigan M-Cubed funds awarded to K.A.S. and G.R.R.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.relation.urihttps://doi.org/10.1002/advs.201500025
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAggregationen_US
dc.subjectBiocrystalsen_US
dc.subjectChromophoresen_US
dc.subjectClofazimineen_US
dc.subjectMedicinal chemistryen_US
dc.titleMassive bioaccumulation and self-assembly of phenazine compounds in live cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/advs.201500025


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as Attribution 4.0 International