| Literature DB >> 26366522 |
Marina Buzhor1,2, Assaf J Harnoy1,2, Einat Tirosh3,2, Ayana Barak3,2, Tal Schwartz3,2, Roey J Amir4,5.
Abstract
The need for advanced fluorescent imaging and delivery platforms has motivated the development of smart probes that change their fluorescence in response to external stimuli. Here a new molecular design of fluorescently labeled PEG-dendron hybrids that self-assemble into enzyme-responsive micelles with tunable fluorescent responses is reported. In the assembled state, the fluorescence of the dyes is quenched or shifted due to intermolecular interactions. Upon enzymatic cleavage of the hydrophobic end-groups, the labeled polymeric hybrids become hydrophilic, and the micelles disassemble. This supramolecular change is translated into a spectral response as the dye-dye interactions are eliminated and the intrinsic fluorescence is regained. We demonstrate the utilization of this molecular design to generate both Turn-On and spectral shift responses by adjusting the type of the labeling dye. This approach enables transformation of non-responsive labeling dyes into smart fluorescent probes.Entities:
Keywords: enzymes; fluorescence; micelles; nanocarriers; stimuli-responsive polymers
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Year: 2015 PMID: 26366522 DOI: 10.1002/chem.201502988
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236