Self-Assembled Gold Nanoparticle Molecular Probes for Detecting Proteolytic Activity

Target-activatable fluorogenic probes based on gold nanoparticles (AuNPs) functionalized with self-assembled heterogeneous monolayers of dye-labeled peptides and poly(ethylene glycol) have been developed to visualize proteolytic activity in vivo. A one-step synthesis strategy that allows simple gene...

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Bibliographic Details
Main Authors: Mu, C. Jenny (Contributor), LaVan, David A. (Author), Langer, Robert (Contributor), Zetter, Bruce R. (Author)
Other Authors: Harvard University- (Contributor), Massachusetts Institute of Technology. Department of Chemical Engineering (Contributor)
Format: Article
Language:English
Published: American Chemical Society, 2013-06-06T19:42:57Z.
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Online Access:Get fulltext
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100 1 0 |a Mu, C. Jenny  |e author 
100 1 0 |a Harvard University-  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Chemical Engineering  |e contributor 
100 1 0 |a Langer, Robert  |e contributor 
100 1 0 |a Mu, C. Jenny  |e contributor 
700 1 0 |a LaVan, David A.  |e author 
700 1 0 |a Langer, Robert  |e author 
700 1 0 |a Zetter, Bruce R.  |e author 
245 0 0 |a Self-Assembled Gold Nanoparticle Molecular Probes for Detecting Proteolytic Activity 
260 |b American Chemical Society,   |c 2013-06-06T19:42:57Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/79074 
520 |a Target-activatable fluorogenic probes based on gold nanoparticles (AuNPs) functionalized with self-assembled heterogeneous monolayers of dye-labeled peptides and poly(ethylene glycol) have been developed to visualize proteolytic activity in vivo. A one-step synthesis strategy that allows simple generation of surface-defined AuNP probe libraries is presented as a means of tailoring and evaluating probe characteristics for maximal fluorescence enhancement after protease activation. Optimal AuNP probes targeted to trypsin and urokinase-type plasminogen activator required the incorporation of a dark quencher to achieve 5- to 8-fold signal amplification. These probes exhibited extended circulation time in vivo and high image contrast in a mouse tumor model. 
520 |a National Institutes of Health (U.S.) (NIH grant CA119402) 
520 |a National Institutes of Health (U.S.) (grant DE013023) 
520 |a National Institutes of Health (U.S.) (grant DE016516) 
520 |a National Science Foundation (U.S.). Materials Research Science and Engineering Centers (Program) (award number DMR-08-19762) 
546 |a en_US 
655 7 |a Article 
773 |t ACS Nano