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The complementary morpholino oligonucleotide to MORF1 (cMORF1) is a synthetic, non-natural nucleic acid analog utilized as a high-affinity probe in pre-targeted nuclear medicine (Liu et al., 2002). It is a member of the phosphorodiamidate morpholino oligomer (PMO) family, which features a backbone of morpholine rings and phosphorodiamidate linkages that are resistant to enzymatic degradation by nucleases (Hnatowich et al., 1996). In a pre-targeting protocol, a primary targeting agent, such as a monoclonal antibody conjugated to the MORF1 sequence, is first administered to bind to a specific disease-associated antigen. Once the primary agent has cleared from the blood, a radiolabeled cMORF1 is injected, which rapidly and specifically hybridizes with the MORF1 sequence at the target site via Watson-Crick base pairing (He et al., 2005). This approach allows for high-contrast imaging and potent radioimmunotherapy by decoupling the slow localization of antibodies from the rapid delivery of the effector molecule, thereby minimizing systemic radiation exposure.
High-affinity hybridization via Watson-Crick base pairing with a complementary MORF1 sequence conjugated to a primary targeting agent.
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