Transglutaminases, including factor XIII and tissue transglutaminase, participate in multiple extracellular processes associated with remodeling of the extracellular matrix during wound repair, blood clotting, tumor progression and fibrosis of ischemic injuries. The aim of this work was to evaluate a novel substrate analog for transglutaminase optimized by molecular modeling calculations (DCCP16), which can serve for molecular imaging of transglutaminase activity by magnetic resonance imaging and by near-infrared imaging. Experimental data showed covalent binding of Gd-DCCP16 and DCCP16-IRIS Blue to human clots, to basement membrane components and to casein in purified systems as well as in three-dimensional multicellular spheroids. In vivo, DCCP16 showed enhancement with a prolonged retention in clots and tumors, demonstrating the ability to detect both factor XIII and tissue transglutaminase mediated covalent binding of the contrast material.
Contrast Media/chemistry , Coordination Complexes/chemistry , Factor XIII/chemistry , Fluorescent Dyes/chemistry , Indoles/chemistry , Magnetic Resonance Imaging , Peptides/chemistry , Transglutaminases/metabolism , Animals , Factor XIII/metabolism , Humans , Mice , Mice, Inbred Strains , Spheroids, Cellular/metabolism , Transglutaminases/chemistry
