Genetically targeted fluorogenic macromolecules for subcellular imaging and cellular perturbation

被引:8
|
作者
Magenau, Andrew J. D. [1 ,2 ]
Saurabh, Saumya [2 ]
Andreko, Susan K. [1 ]
Telmer, Cheryl A. [1 ,3 ]
Schmidt, Brigitte F. [1 ]
Waggoner, Alan S. [1 ,3 ]
Bruchez, Marcel P. [1 ,2 ,3 ]
机构
[1] Carnegie Mellon Univ, Mol Biosensors & Imaging Ctr, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
关键词
Polymer modified cells; Targeting polymers to subcellular organelles; Genetically targetable macromolecules; Subcellular imaging; Protein polymer hybrids; Biomaterial structure-property relationships; Atom transfer radical polymerization (ATRP); Fluorogen-activating proteins (FAPs); FREE-RADICAL POLYMERIZATION; DRUG-DELIVERY; NANOPARTICLES; BINDING; DESIGN; PROTEINS; TRACKING;
D O I
10.1016/j.biomaterials.2015.07.002
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 per-meabilization 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. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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