Abstract
Among the classical collagenases, matrix metalloproteinase-13 (calledMMP-13, collagenase-3) is one of the most important components for cartilage destruction of osteoarthritis (OA) developments. Despite many efforts, the detection methods of MMP-13 activity have been met with limited success in vivo, in part, due to the low sensitivity and low selectivity by homology of MMP family. Previously, we demonstrated the use of strongly dark-quenched fluorogenic probe allowed for the visual detection of MMP- 13 in vitro and in OA-induced rat models. In this study, we described the optimization of MMP-13 fluorogenic probe for OA detection in vivo. Three candidate probes demonstrated recovered fluorescent intensity proportional with MMP-13 concentrations, respectively; however, Probe 2 exhibited both high signal amplification and selective recognition for MMP-13, not MMP-2 and MMP-9 in vitro. When Probe 2 was applied to OA-induced rat models, clear visualization of MMP-13 activity in OA-induced cartilage was obtained. Optimized MMP-13 fluorogenic probe can be applied to detect and image OA and have potential for evaluating the in vivo efficacy of MMP-13 inhibitors which are being tested for therapeutic treatment of OA.
Original language | English |
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Pages (from-to) | 1113-1122 |
Number of pages | 10 |
Journal | Amino Acids |
Volume | 41 |
Issue number | 5 |
DOIs | |
State | Published - Nov 2011 |
Bibliographical note
Funding Information:This work was financially supported by the Real-Time Molecular Imaging Project, GRL program, and the Pioneer Research Program for Covering Technology of MEST and by a grant to the Intramural Research Program (Theragnosis) of the KIST, and by a grant (A062254) of the Korea Health 21 R&D Project.
Keywords
- Fluorogenic probe
- Matrix metalloproteinase (MMP)
- Optical imaging
- Osteoarthritis
- Peptide