Initial characterization of a dually radiolabeled peptide for simultaneous monitoring of protein targets and enzymatic activity

摘要

Objective: The goal of this study was to develop dually radiolabeled peptides for simultaneous imaging of cancer cell localization by targeting the ??v??3 integrin and their pathophysiology by targeting the activity of the proteolytic enzyme MMP2, involved in the metastatic process. Methods: A hybrid peptide c(RGDfE)K(DOTA)PLGVRY containing an RGD motif for binding to the ??v??3integrin, a metal chelator (DOTA) for radiolabeling with [64Cu], and the MMP2 substrate cleavage sequence PLGVRY with terminal tyrosine for labeling with [123I] was synthesized, labeled with [64Cu] and [123I], and evaluated in vitro as a potential imaging agent. Results: The peptide was synthesized and labeled with [64Cu] and [123I] with 300 and 40??Ci/??g (542 and 72.2mCi/??mol) specific activities, respectively, and radiochemical purity of 98%. c(RGDfE)K(DOTA)PLGVRY demonstrated high affinity for ??v??3 integrins (Kd=83.4+13.2nM) in both substrate competition and cell binding assays. c(RGDfE)K(DOTA)PLGVRY peptide, but not the scrambled version, c(RGDfE)K(DOTA)GRPLVY was specifically cleaved by MMP2. Conclusions: These results demonstrate the feasibility of developing dually radiolabeled peptides for the simultaneous imaging of cancer cells and their pathophysiologic activity. ? 2013 Elsevier Inc.