Premium
In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin S Substrate
Author(s) -
Hu HaiYu,
Vats Divya,
Vizovisek Matej,
Kramer Lovro,
Germanier Catherine,
Wendt K. Ulrich,
Rudin Markus,
Turk Boris,
Plettenburg Oliver,
Schultz Carsten
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201310979
Subject(s) - cleavage (geology) , cathepsin , chemistry , intracellular , in vivo , fluorescence , microbiology and biotechnology , lipid anchored protein , biophysics , biochemistry , biology , enzyme , apoptosis , paleontology , physics , autophagy , quantum mechanics , fracture (geology)
The synthesis and evaluation of two cathepsin S‐specific probes is described. For long‐term retention of the probe at the target site and a high signal‐to‐noise ratio, we introduced a lipidation approach via the simple attachment of palmitoic acid to the reporter. After cathepsin S‐specific cleavage in cultured cells and in a grafted tumor mouse model, fluorescence increased owing to dequenching and we observed an intracellular accumulation of the fluorescence in the target tissue. The lipidated probe provided a prolonged and strongly fluorescent signal in tumors when compared to the very similar non‐lipidated probe, demonstrating that non‐invasive tumor identification is feasable. The homing principle by probe lipidation might also work for selective administration of cytotoxic compounds to specifically reduce tumor mass.