Improved quenched fluorescent probe for imaging of cysteine cathepsin activity.

J Am Chem Soc

Departments of †Pathology, ‡Cancer Biology Program, and §Microbiology and Immunology, Stanford School of Medicine, 300 Pasteur Drive, Stanford, California 94305-5324, United States.

Published: October 2013

The cysteine cathepsins are a family of proteases that play important roles in both normal cellular physiology and many human diseases. In cancer, the activity of many of the cysteine cathepsins is upregulated and can be exploited for tumor imaging. Here we present the design and synthesis of a new class of quenched fluorescent activity-based probes (qABPs) containing a phenoxymethyl ketone (PMK) electrophile. These reagents show enhanced in vivo properties and broad reactivity resulting in dramatically improved labeling and tumor imaging properties compared to those of previously reported ABPs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826460PMC
http://dx.doi.org/10.1021/ja4056068DOI Listing

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