| Literature DB >> 26183934 |
Andrew J D Magenau1, Saumya Saurabh2, Susan K Andreko3, Cheryl A Telmer4, Brigitte F Schmidt3, Alan S Waggoner4, Marcel P Bruchez5.
Abstract
The alteration of cellular functions by anchoring macromolecules to specified organelles may reveal a new area of therapeutic potential and clinical treatment. In this work, a unique phenotype was evoked by influencing cellular behavior through the modification of subcellular structures with genetically targetable macromolecules. These fluorogen-functionalized polymers, prepared via controlled radical polymerization, were capable of exclusively decorating actin, cytoplasmic, or nuclear compartments of living cells expressing localized fluorgen-activating proteins. The macromolecular fluorogens were optimized by establishing critical polymer architecture-biophysical property relationships which impacted binding rates, binding affinities, and the level of internalization. Specific labeling of subcellular structures was realized at nanomolar concentrations of polymer, in the absence of membrane permeabilization or transduction domains, and fluorogen-modified polymers were found to bind to protein intact after delivery to the cytosol. Cellular motility was found to be dependent on binding of macromolecular fluorogens to actin structures causing rapid cellular ruffling without migration.Entities:
Keywords: Atom transfer radical polymerization (ATRP); Biomaterial structure-property relationships; Fluorogen-activating proteins (FAPs); Genetically targetable macromolecules; Polymer modified cells; Protein polymer hybrids; Subcellular imaging; Targeting polymers to subcellular organelles
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Year: 2015 PMID： 26183934 PMCID： PMC4522379 DOI： 10.1016/j.biomaterials.2015.07.002
Source DB: PubMed Journal: Biomaterials ISSN： 0142-9612 Impact factor: 12.479