Novel affibody molecules as potential agents in molecular imaging for MAGE-A3-positive tumor diagnosis

Background The cancer-testis protein melanoma antigen A3 (MAGE-A3) is highly expressed in a broad range of malignant tumor forms. It has been confirmed that affibody molecules, a novel family of small (?6.5?kDa) targeting proteins, are useful agents for molecular imaging and targeted tumor treatment. As a novel agent for in vivo molecular imaging detection of MAGE-A3-positive tumors, the efficacy of affibody molecules was assessed in this research. Methods In this study, three cycles of phage display library screening resulted in the isolation of two new affibody molecules (Z MAGE-A3 :172 and Z MAGE-A3 :770) that attach to MAGE-A3. These molecules were then expressed in bacteria and purified. The affibody molecules with high affinity and specificity were evaluated using western blotting, immunohistochemistry, indirect immunofluorescence, surface plasmon resonance , and near-infrared optical imaging of tumor-bearing nude mice. Results The selected Z MAGE-A3 affibodies can precisely bind to the MAGE-A3 protein in living cells and display high-affinity binding to the MAGE-A3 protein at the molecular level. Furthermore, the accumulation of DyLight755-labeled Z MAGE-A3 :172 or Z MAGE-A3 :770 in MAGE-A3-positive tumors was achieved as early as 30?min and disappeared at 48?h post-injection. Conclusion Our findings support the potential of the two MAGE-A3 protein-binding affibody molecules for their use as molecular imaging agents.

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